ENST00000338034.9:c.2416G>T
MANE Select
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ENSP00000337445.4:p.Gly806Trp
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ENST00000338034.8:c.2416G>T
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ENSP00000337445.4:p.Gly806Trp
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ENST00000395962.6:c.2359G>T
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ENSP00000379291.1:p.Gly787Trp
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ENST00000426905.7:c.2296G>T
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ENSP00000405223.3:p.Gly766Trp
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ENST00000465825.5:n.2303G>T
|
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ENST00000480891.5:n.2245G>T
|
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ENST00000484122.5:n.3246G>T
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ENST00000487229.6:n.1962G>T
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|
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ENST00000584650.5:c.1815G>T
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NM_001165962.1:c.2296G>T
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NP_001159434.1:p.Gly766Trp
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NM_018127.6:c.2416G>T
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NP_060597.4:p.Gly806Trp
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NM_173717.1:c.2413G>T
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NP_776065.1:p.Gly805Trp
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XM_024450850.1:c.2575G>T
|
XP_024306618.1:p.Gly859Trp
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XM_024450851.1:c.2497G>T
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XP_024306619.1:p.Gly833Trp
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XM_024450852.1:c.2494G>T
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XP_024306620.1:p.Gly832Trp
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XM_024450853.1:c.2491G>T
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XP_024306621.1:p.Gly831Trp
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XM_024450854.1:c.2455G>T
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XP_024306622.1:p.Gly819Trp
|
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XM_024450855.1:c.2374G>T
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XP_024306623.1:p.Gly792Trp
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XM_024450856.1:c.2293G>T
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XP_024306624.1:p.Gly765Trp
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XM_024450857.1:c.2293G>T
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XP_024306625.1:p.Gly765Trp
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XM_024450858.1:c.2212G>T
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XP_024306626.1:p.Gly738Trp
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XM_024450859.1:c.2209G>T
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XP_024306627.1:p.Gly737Trp
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XM_024450860.1:c.2134G>T
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XP_024306628.1:p.Gly712Trp
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XM_024450861.1:c.2134G>T
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XP_024306629.1:p.Gly712Trp
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XM_024450862.1:c.2131G>T
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XP_024306630.1:p.Gly711Trp
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NM_018127.7:c.2416G>T
MANE Select
|
NP_060597.4:p.Gly806Trp
|
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NM_001165962.2:c.2296G>T
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NP_001159434.1:p.Gly766Trp
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NM_173717.2:c.2413G>T
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NP_776065.1:p.Gly805Trp
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