ENST00000703783.1:n.1121C>A
|
|
|
ENST00000703785.1:n.1202C>A
|
|
|
ENST00000262464.9:c.4337C>A
MANE Select
|
ENSP00000262464.4:p.Thr1446Asn
|
|
ENST00000262464.8:c.4337C>A
|
ENSP00000262464.4:p.Thr1446Asn
|
|
ENST00000507835.5:c.887C>A
|
ENSP00000426839.1:p.Thr296Asn
|
|
ENST00000508053.5:c.4337C>A
|
ENSP00000424571.1:p.Thr1446Asn
|
|
ENST00000508989.5:c.4238C>A
|
ENSP00000425596.1:p.Thr1413Asn
|
|
ENST00000619499.4:c.4334C>A
|
ENSP00000482132.1:p.Thr1445Asn
|
|
NM_001999.3:c.4337C>A
|
NP_001990.2:p.Thr1446Asn
|
|
XM_017009228.2:c.4184C>A
|
XP_016864717.1:p.Thr1395Asn
|
|
NM_001999.4:c.4337C>A
MANE Select
|
NP_001990.2:p.Thr1446Asn
|
|