ENST00000334504.12:c.5058T>A
MANE Select
|
ENSP00000334733.7:p.Cys1686Ter
|
|
ENST00000334504.11:c.5058T>A
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ENSP00000334733.7:p.Cys1686Ter
|
|
ENST00000372216.8:c.5061T>A
|
ENSP00000361290.4:p.Cys1687Ter
|
|
ENST00000394872.6:c.5109T>A
|
ENSP00000378340.3:p.Cys1703Ter
|
|
ENST00000538570.5:c.4887T>A
|
ENSP00000445236.1:p.Cys1629Ter
|
|
ENST00000545689.2:c.5022T>A
|
ENSP00000443707.2:p.Cys1674Ter
|
|
ENST00000621266.4:c.4986T>A
|
ENSP00000482970.1:p.Cys1662Ter
|
|
NM_001287758.1:c.5109T>A
|
NP_001274687.1:p.Cys1703Ter
|
|
NM_001287759.1:c.4986T>A
|
NP_001274688.1:p.Cys1662Ter
|
|
NM_001287760.1:c.4887T>A
|
NP_001274689.1:p.Cys1629Ter
|
|
NM_001847.3:c.5061T>A
|
NP_001838.2:p.Cys1687Ter
|
|
NM_033641.3:c.5058T>A
|
NP_378667.1:p.Cys1686Ter
|
|
XM_006724617.2:c.5112T>A
|
XP_006724680.1:p.Cys1704Ter
|
|
XM_011530852.1:c.5040T>A
|
XP_011529154.1:p.Cys1680Ter
|
|
XM_011530853.1:c.5028T>A
|
XP_011529155.1:p.Cys1676Ter
|
|
XM_006724617.3:c.5112T>A
|
XP_006724680.1:p.Cys1704Ter
|
|
XM_011530852.2:c.5040T>A
|
XP_011529154.1:p.Cys1680Ter
|
|
XM_011530853.3:c.5028T>A
|
XP_011529155.1:p.Cys1676Ter
|
|
NM_001847.4:c.5061T>A
|
NP_001838.2:p.Cys1687Ter
|
|
NM_033641.4:c.5058T>A
MANE Select
|
NP_378667.1:p.Cys1686Ter
|
|
NM_001287758.2:c.5109T>A
|
NP_001274687.1:p.Cys1703Ter
|
|
NM_001287759.2:c.4986T>A
|
NP_001274688.1:p.Cys1662Ter
|
|
NM_001287760.2:c.4887T>A
|
NP_001274689.1:p.Cys1629Ter
|
|