ENST00000703783.1:n.539G>T
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|
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ENST00000703785.1:n.620G>T
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ENST00000262464.9:c.3755G>T
MANE Select
|
ENSP00000262464.4:p.Gly1252Val
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ENST00000262464.8:c.3755G>T
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ENSP00000262464.4:p.Gly1252Val
|
|
ENST00000507835.5:c.305G>T
|
ENSP00000426839.1:p.Gly102Val
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ENST00000508053.5:c.3755G>T
|
ENSP00000424571.1:p.Gly1252Val
|
|
ENST00000508989.5:c.3656G>T
|
ENSP00000425596.1:p.Gly1219Val
|
|
ENST00000619499.4:c.3752G>T
|
ENSP00000482132.1:p.Gly1251Val
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|
NM_001999.3:c.3755G>T
|
NP_001990.2:p.Gly1252Val
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|
XM_017009228.2:c.3602G>T
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XP_016864717.1:p.Gly1201Val
|
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NM_001999.4:c.3755G>T
MANE Select
|
NP_001990.2:p.Gly1252Val
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