ENST00000223051.8:c.1906G>T
MANE Select
|
ENSP00000223051.3:p.Asp636Tyr
|
|
ENST00000223051.7:c.1906G>T
|
ENSP00000223051.3:p.Asp636Tyr
|
|
ENST00000431692.5:c.*581G>T
|
ENSP00000413905.1:n.*581G>T
|
|
ENST00000461176.1:n.252G>T
|
|
|
ENST00000462090.5:n.942G>T
|
|
|
ENST00000462107.1:c.1906G>T
|
ENSP00000420525.1:p.Asp636Tyr
|
|
ENST00000465294.5:n.1826G>T
|
|
|
ENST00000476304.5:n.1527G>T
|
|
|
ENST00000490084.5:c.1259G>T
|
|
|
NM_001206855.1:c.1393G>T
|
NP_001193784.1:p.Asp465Tyr
|
|
NM_003227.3:c.1906G>T
|
NP_003218.2:p.Asp636Tyr
|
|
XM_005250553.3:c.1906G>T
|
XP_005250610.1:p.Asp636Tyr
|
|
XM_005250554.3:c.1906G>T
|
XP_005250611.1:p.Asp636Tyr
|
|
XR_927814.1:n.434-3803C>A
|
|
|
NM_001206855.2:c.1393G>T
|
NP_001193784.1:p.Asp465Tyr
|
|
XM_005250553.4:c.1906G>T
|
XP_005250610.1:p.Asp636Tyr
|
|
XM_017012573.1:c.1906G>T
|
XP_016868062.1:p.Asp636Tyr
|
|
NM_003227.4:c.1906G>T
MANE Select
|
NP_003218.2:p.Asp636Tyr
|
|
NM_001206855.3:c.1393G>T
|
NP_001193784.1:p.Asp465Tyr
|
|