ENST00000455537.7:c.2938G>T
MANE Select
|
ENSP00000408979.2:p.Ala980Ser
|
|
ENST00000674619.1:c.2959G>T
|
ENSP00000502270.1:p.Ala987Ser
|
|
ENST00000675697.1:c.29G>T
|
|
|
ENST00000675737.1:n.342G>T
|
|
|
ENST00000675882.1:n.2461G>T
|
|
|
ENST00000675929.1:n.1496G>T
|
|
|
ENST00000676055.1:c.29G>T
|
|
|
ENST00000676457.1:c.2833G>T
|
ENSP00000501588.1:p.Ala945Ser
|
|
ENST00000286452.5:c.2671G>T
|
ENSP00000286452.5:p.Ala891Ser
|
|
ENST00000455537.6:c.2938G>T
|
ENSP00000408979.2:p.Ala980Ser
|
|
ENST00000552227.1:n.221G>T
|
|
|
NM_004984.2:c.2938G>T
|
NP_004975.2:p.Ala980Ser
|
|
NM_001354705.1:c.2671G>T
|
NP_001341634.1:p.Ala891Ser
|
|
NM_004984.3:c.2938G>T
|
NP_004975.2:p.Ala980Ser
|
|
XR_002957324.1:n.3171G>T
|
|
|
NM_004984.4:c.2938G>T
MANE Select
|
NP_004975.2:p.Ala980Ser
|
|
NM_001354705.2:c.2671G>T
|
NP_001341634.1:p.Ala891Ser
|
|