ENST00000338037.11:c.2055T>G
MANE Select
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ENSP00000338185.6:p.Gly685=
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ENST00000635830.1:n.2126T>G
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|
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ENST00000636825.1:n.1919T>G
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ENST00000637919.1:c.1752T>G
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ENSP00000490862.1:p.Gly584=
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ENST00000338037.10:c.2055T>G
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ENSP00000338185.6:p.Gly685=
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ENST00000378637.6:c.2055T>G
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ENSP00000367904.2:p.Gly685=
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ENST00000378641.7:c.2055T>G
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ENSP00000367908.3:p.Gly685=
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ENST00000439627.2:c.12T>G
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ENSP00000391162.1:p.Gly4=
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ENST00000487210.5:c.1277T>G
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|
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ENST00000494924.2:n.1207T>G
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ENST00000612075.4:c.1815T>G
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ENSP00000479997.1:p.Gly605=
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ENST00000617005.4:c.1815T>G
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ENSP00000477664.1:p.Gly605=
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ENST00000625874.2:c.1752T>G
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ENSP00000486301.1:p.Gly584=
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ENST00000626966.2:c.1752T>G
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ENSP00000487075.1:p.Gly584=
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NM_015192.3:c.2055T>G
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NP_056007.1:p.Gly685=
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NM_182734.2:c.2055T>G
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NP_877398.1:p.Gly685=
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XM_011529199.1:c.2055T>G
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XP_011527501.1:p.Gly685=
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XM_011529200.1:c.1839T>G
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XP_011527502.1:p.Gly613=
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XM_011529201.1:c.1752T>G
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XP_011527503.1:p.Gly584=
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XM_011529203.1:c.282T>G
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XP_011527505.1:p.Gly94=
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NM_015192.4:c.2055T>G
MANE Select
|
NP_056007.1:p.Gly685=
|
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NM_182734.3:c.2055T>G
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NP_877398.1:p.Gly685=
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