ENST00000377833.10:c.10745C>A
MANE Select
|
ENSP00000367064.4:p.Ser3582Tyr
|
|
ENST00000377833.8:c.10745C>A
|
ENSP00000367064.4:p.Ser3582Tyr
|
|
NM_001081.3:c.10745C>A , LRG_540t1:c.10745C>A
|
NP_001072.2:p.Ser3582Tyr
|
|
XM_011519709.1:c.6731C>A
|
XP_011518011.1:p.Ser2244Tyr
|
|
XM_011519710.1:c.6707C>A
|
XP_011518012.1:p.Ser2236Tyr
|
|
XM_011519711.1:c.6587C>A
|
XP_011518013.1:p.Ser2196Tyr
|
|
XM_011519709.2:c.6731C>A
|
XP_011518011.1:p.Ser2244Tyr
|
|
XM_011519710.2:c.6707C>A
|
XP_011518012.1:p.Ser2236Tyr
|
|
XM_011519711.3:c.6587C>A
|
XP_011518013.1:p.Ser2196Tyr
|
|
NM_001081.4:c.10745C>A
MANE Select
|
NP_001072.2:p.Ser3582Tyr
|
|