ENST00000216075.11:c.820C>T
MANE Select
|
ENSP00000216075.6:p.Leu274Phe
|
|
ENST00000216075.10:c.820C>T
|
ENSP00000216075.6:p.Leu274Phe
|
|
ENST00000395732.7:c.806C>T
|
ENSP00000379081.3:p.Ala269Val
|
|
ENST00000395733.7:c.689C>T
|
ENSP00000379082.3:p.Ala230Val
|
|
ENST00000451761.1:c.760C>T
|
ENSP00000409894.1:p.Leu254Phe
|
|
NM_017584.5:c.820C>T
|
NP_060054.4:p.Leu274Phe
|
|
XM_005261925.3:c.682C>T
|
XP_005261982.1:p.Leu228Phe
|
|
XR_244455.2:n.3316C>T
|
|
|
XM_005261925.4:c.682C>T
|
XP_005261982.1:p.Leu228Phe
|
|
NM_017584.6:c.820C>T
MANE Select
|
NP_060054.4:p.Leu274Phe
|
|