ENST00000541682.7:c.372C>T
MANE Select
|
ENSP00000446205.2:p.Phe124=
|
|
ENST00000317814.8:c.357C>T
|
ENSP00000314774.4:p.Phe119=
|
|
ENST00000541682.6:c.372C>T
|
ENSP00000446205.2:p.Phe124=
|
|
ENST00000577735.1:c.348C>T
|
ENSP00000462491.1:p.Phe116=
|
|
NM_001165967.1:c.372C>T
|
NP_001159439.1:p.Phe124=
|
|
NM_032580.3:c.357C>T
|
NP_115969.2:p.Phe119=
|
|
XM_011524038.1:c.477C>T
|
XP_011522340.1:p.Phe159=
|
|
XM_011524039.1:c.468C>T
|
XP_011522341.1:p.Phe156=
|
|
XM_011524040.1:c.468C>T
|
XP_011522342.1:p.Phe156=
|
|
XM_011524041.1:c.459C>T
|
XP_011522343.1:p.Phe153=
|
|
XM_011524042.1:c.330C>T
|
XP_011522344.1:p.Phe110=
|
|
XR_934203.1:n.69+2078G>A
|
|
|
XM_017025232.1:c.477C>T
|
XP_016880721.1:p.Phe159=
|
|
XM_024451007.1:c.477C>T
|
XP_024306775.1:p.Phe159=
|
|
NM_001165967.2:c.372C>T
MANE Select
|
NP_001159439.1:p.Phe124=
|
|
NM_032580.4:c.357C>T
|
NP_115969.2:p.Phe119=
|
|