ENST00000541682.7:c.302T>A
MANE Select
|
ENSP00000446205.2:p.Phe101Tyr
|
|
ENST00000317814.8:c.287T>A
|
ENSP00000314774.4:p.Phe96Tyr
|
|
ENST00000541682.6:c.302T>A
|
ENSP00000446205.2:p.Phe101Tyr
|
|
ENST00000577735.1:c.278T>A
|
ENSP00000462491.1:p.Phe93Tyr
|
|
NM_001165967.1:c.302T>A
|
NP_001159439.1:p.Phe101Tyr
|
|
NM_032580.3:c.287T>A
|
NP_115969.2:p.Phe96Tyr
|
|
XM_011524038.1:c.407T>A
|
XP_011522340.1:p.Phe136Tyr
|
|
XM_011524039.1:c.398T>A
|
XP_011522341.1:p.Phe133Tyr
|
|
XM_011524040.1:c.398T>A
|
XP_011522342.1:p.Phe133Tyr
|
|
XM_011524041.1:c.389T>A
|
XP_011522343.1:p.Phe130Tyr
|
|
XM_011524042.1:c.260T>A
|
XP_011522344.1:p.Phe87Tyr
|
|
XR_934203.1:n.69+2148A>T
|
|
|
XM_017025232.1:c.407T>A
|
XP_016880721.1:p.Phe136Tyr
|
|
XM_024451007.1:c.407T>A
|
XP_024306775.1:p.Phe136Tyr
|
|
NM_001165967.2:c.302T>A
MANE Select
|
NP_001159439.1:p.Phe101Tyr
|
|
NM_032580.4:c.287T>A
|
NP_115969.2:p.Phe96Tyr
|
|