ENST00000377833.10:c.5840C>A
MANE Select
|
ENSP00000367064.4:p.Ser1947Tyr
|
|
ENST00000377833.8:c.5840C>A
|
ENSP00000367064.4:p.Ser1947Tyr
|
|
NM_001081.3:c.5840C>A , LRG_540t1:c.5840C>A
|
NP_001072.2:p.Ser1947Tyr
|
|
XM_011519708.1:c.5840C>A
|
XP_011518010.1:p.Ser1947Tyr
|
|
XM_011519709.1:c.1826C>A
|
XP_011518011.1:p.Ser609Tyr
|
|
XM_011519710.1:c.1802C>A
|
XP_011518012.1:p.Ser601Tyr
|
|
XM_011519711.1:c.1682C>A
|
XP_011518013.1:p.Ser561Tyr
|
|
XM_011519708.2:c.5840C>A
|
XP_011518010.1:p.Ser1947Tyr
|
|
XM_011519709.2:c.1826C>A
|
XP_011518011.1:p.Ser609Tyr
|
|
XM_011519710.2:c.1802C>A
|
XP_011518012.1:p.Ser601Tyr
|
|
XM_011519711.3:c.1682C>A
|
XP_011518013.1:p.Ser561Tyr
|
|
NM_001081.4:c.5840C>A
MANE Select
|
NP_001072.2:p.Ser1947Tyr
|
|