ENST00000703783.1:n.1086T>A
|
|
|
ENST00000703785.1:n.1167T>A
|
|
|
ENST00000262464.9:c.4302T>A
MANE Select
|
ENSP00000262464.4:p.Cys1434Ter
|
|
ENST00000262464.8:c.4302T>A
|
ENSP00000262464.4:p.Cys1434Ter
|
|
ENST00000507835.5:c.852T>A
|
ENSP00000426839.1:p.Cys284Ter
|
|
ENST00000508053.5:c.4302T>A
|
ENSP00000424571.1:p.Cys1434Ter
|
|
ENST00000508989.5:c.4203T>A
|
ENSP00000425596.1:p.Cys1401Ter
|
|
ENST00000619499.4:c.4299T>A
|
ENSP00000482132.1:p.Cys1433Ter
|
|
NM_001999.3:c.4302T>A
|
NP_001990.2:p.Cys1434Ter
|
|
XM_017009228.2:c.4149T>A
|
XP_016864717.1:p.Cys1383Ter
|
|
NM_001999.4:c.4302T>A
MANE Select
|
NP_001990.2:p.Cys1434Ter
|
|