ENST00000703783.1:n.194G=
|
|
|
ENST00000703785.1:n.275G=
|
|
|
ENST00000262464.9:c.3410G=
MANE Select
|
ENSP00000262464.4:p.Ser1137=
|
|
ENST00000262464.8:c.3410G=
|
ENSP00000262464.4:p.Ser1137=
|
|
ENST00000507835.5:c.-41G=
|
ENSP00000426839.1:n.-41G=
|
|
ENST00000508053.5:c.3410G=
|
ENSP00000424571.1:p.Ser1137=
|
|
ENST00000508989.5:c.3311G=
|
ENSP00000425596.1:p.Ser1104=
|
|
ENST00000619499.4:c.3407G=
|
ENSP00000482132.1:p.Ser1136=
|
|
NM_001999.3:c.3410G=
|
NP_001990.2:p.Ser1137=
|
|
XM_017009228.2:c.3257G=
|
XP_016864717.1:p.Ser1086=
|
|
NM_001999.4:c.3410G=
MANE Select
|
NP_001990.2:p.Ser1137=
|
|