ENST00000703783.1:n.1128A>C
|
|
|
ENST00000703785.1:n.1209A>C
|
|
|
ENST00000262464.9:c.4344A>C
MANE Select
|
ENSP00000262464.4:p.Ser1448=
|
|
ENST00000262464.8:c.4344A>C
|
ENSP00000262464.4:p.Ser1448=
|
|
ENST00000507835.5:c.894A>C
|
ENSP00000426839.1:p.Ser298=
|
|
ENST00000508053.5:c.4344A>C
|
ENSP00000424571.1:p.Ser1448=
|
|
ENST00000508989.5:c.4245A>C
|
ENSP00000425596.1:p.Ser1415=
|
|
ENST00000619499.4:c.4341A>C
|
ENSP00000482132.1:p.Ser1447=
|
|
NM_001999.3:c.4344A>C
|
NP_001990.2:p.Ser1448=
|
|
XM_017009228.2:c.4191A>C
|
XP_016864717.1:p.Ser1397=
|
|
NM_001999.4:c.4344A>C
MANE Select
|
NP_001990.2:p.Ser1448=
|
|