ENST00000703783.1:n.1031C=
|
|
|
ENST00000703785.1:n.1112C=
|
|
|
ENST00000262464.9:c.4247C=
MANE Select
|
ENSP00000262464.4:p.Thr1416=
|
|
ENST00000262464.8:c.4247C=
|
ENSP00000262464.4:p.Thr1416=
|
|
ENST00000507835.5:c.797C=
|
ENSP00000426839.1:p.Thr266=
|
|
ENST00000508053.5:c.4247C=
|
ENSP00000424571.1:p.Thr1416=
|
|
ENST00000508989.5:c.4148C=
|
ENSP00000425596.1:p.Thr1383=
|
|
ENST00000619499.4:c.4244C=
|
ENSP00000482132.1:p.Thr1415=
|
|
NM_001999.3:c.4247C=
|
NP_001990.2:p.Thr1416=
|
|
XM_017009228.2:c.4094C=
|
XP_016864717.1:p.Thr1365=
|
|
NM_001999.4:c.4247C=
MANE Select
|
NP_001990.2:p.Thr1416=
|
|