ENST00000703783.1:n.991G>T
|
|
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ENST00000703785.1:n.1072G>T
|
|
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ENST00000262464.9:c.4207G>T
MANE Select
|
ENSP00000262464.4:p.Gly1403Cys
|
|
ENST00000262464.8:c.4207G>T
|
ENSP00000262464.4:p.Gly1403Cys
|
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ENST00000507835.5:c.757G>T
|
ENSP00000426839.1:p.Gly253Cys
|
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ENST00000508053.5:c.4207G>T
|
ENSP00000424571.1:p.Gly1403Cys
|
|
ENST00000508989.5:c.4108G>T
|
ENSP00000425596.1:p.Gly1370Cys
|
|
ENST00000619499.4:c.4204G>T
|
ENSP00000482132.1:p.Gly1402Cys
|
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NM_001999.3:c.4207G>T
|
NP_001990.2:p.Gly1403Cys
|
|
XM_017009228.2:c.4054G>T
|
XP_016864717.1:p.Gly1352Cys
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|
NM_001999.4:c.4207G>T
MANE Select
|
NP_001990.2:p.Gly1403Cys
|
|