ENST00000398752.11:c.897T>C
MANE Select
|
ENSP00000381736.5:p.Tyr299=
|
|
ENST00000282050.6:c.897T>C
|
ENSP00000282050.2:p.Tyr299=
|
|
ENST00000398752.10:c.897T>C
|
ENSP00000381736.5:p.Tyr299=
|
|
ENST00000586523.1:n.1302T>C
|
|
|
ENST00000586592.5:c.*960T>C
|
ENSP00000466275.3:n.*960T>C
|
|
ENST00000590156.5:c.*793T>C
|
ENSP00000466309.1:n.*793T>C
|
|
ENST00000590665.5:c.831T>C
|
ENSP00000467037.1:p.Tyr277=
|
|
ENST00000592364.5:c.227-331T>C
|
ENSP00000468618.1:n.227-331T>C
|
|
ENST00000593152.6:c.747T>C
|
ENSP00000465477.2:p.Tyr249=
|
|
NM_001001935.2:c.747T>C
|
NP_001001935.1:p.Tyr249=
|
|
NM_001001937.1:c.897T>C
|
NP_001001937.1:p.Tyr299=
|
|
NM_001257334.1:c.831T>C
|
NP_001244263.1:p.Tyr277=
|
|
NM_001257335.1:c.747T>C
|
NP_001244264.1:p.Tyr249=
|
|
NM_004046.5:c.897T>C
|
NP_004037.1:p.Tyr299=
|
|
XM_011526018.1:c.747T>C
|
XP_011524320.1:p.Tyr249=
|
|
XM_017025789.1:c.897T>C
|
XP_016881278.1:p.Tyr299=
|
|
NM_004046.6:c.897T>C
MANE Select
|
NP_004037.1:p.Tyr299=
|
|
NM_001001935.3:c.747T>C
|
NP_001001935.1:p.Tyr249=
|
|
NM_001257334.2:c.831T>C
|
NP_001244263.1:p.Tyr277=
|
|
NM_001001937.2:c.897T>C
|
NP_001001937.1:p.Tyr299=
|
|
NM_001257335.2:c.747T>C
|
NP_001244264.1:p.Tyr249=
|
|