ENST00000683572.1:n.703G>T
|
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ENST00000341947.7:c.4897G>T
MANE Select
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ENSP00000339915.2:p.Gly1633Cys
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ENST00000341947.6:c.4897G>T
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ENSP00000339915.2:p.Gly1633Cys
|
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ENST00000361917.5:c.4576G>T
|
ENSP00000355123.1:p.Gly1526Cys
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ENST00000374708.8:c.4639G>T
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ENSP00000363840.4:p.Gly1547Cys
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ENST00000477772.1:n.687G>T
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|
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NM_080679.2:c.4576G>T
|
NP_542410.2:p.Gly1526Cys
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NM_080680.2:c.4897G>T
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NP_542411.2:p.Gly1633Cys
|
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NM_080681.2:c.4639G>T
|
NP_542412.2:p.Gly1547Cys
|
|
XM_011514298.1:c.4051G>T
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XP_011512600.1:p.Gly1351Cys
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XM_011514299.1:c.4183G>T
|
XP_011512601.1:p.Gly1395Cys
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XM_011514300.1:c.4003G>T
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XP_011512602.1:p.Gly1335Cys
|
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XM_011514301.1:c.3940G>T
|
XP_011512603.1:p.Gly1314Cys
|
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XM_011514302.1:c.3784G>T
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XP_011512604.1:p.Gly1262Cys
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|
XM_011514299.2:c.4183G>T
|
XP_011512601.1:p.Gly1395Cys
|
|
XM_011514300.2:c.4003G>T
|
XP_011512602.1:p.Gly1335Cys
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XM_011514302.2:c.3784G>T
|
XP_011512604.1:p.Gly1262Cys
|
|
XM_017010250.1:c.4897G>T
|
XP_016865739.1:p.Gly1633Cys
|
|
XM_017010251.2:c.3715G>T
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XP_016865740.1:p.Gly1239Cys
|
|
NM_080680.3:c.4897G>T
MANE Select
|
NP_542411.2:p.Gly1633Cys
|
|
NM_080681.3:c.4639G>T
|
NP_542412.2:p.Gly1547Cys
|
|
NM_080679.3:c.4576G>T
|
NP_542410.2:p.Gly1526Cys
|
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