ENST00000683572.1:n.797T>G
|
|
|
ENST00000341947.7:c.4991T>G
MANE Select
|
ENSP00000339915.2:p.Leu1664Arg
|
|
ENST00000341947.6:c.4991T>G
|
ENSP00000339915.2:p.Leu1664Arg
|
|
ENST00000361917.5:c.4670T>G
|
ENSP00000355123.1:p.Leu1557Arg
|
|
ENST00000374708.8:c.4733T>G
|
ENSP00000363840.4:p.Leu1578Arg
|
|
ENST00000477772.1:n.781T>G
|
|
|
NM_080679.2:c.4670T>G
|
NP_542410.2:p.Leu1557Arg
|
|
NM_080680.2:c.4991T>G
|
NP_542411.2:p.Leu1664Arg
|
|
NM_080681.2:c.4733T>G
|
NP_542412.2:p.Leu1578Arg
|
|
XM_011514298.1:c.4145T>G
|
XP_011512600.1:p.Leu1382Arg
|
|
XM_011514299.1:c.4277T>G
|
XP_011512601.1:p.Leu1426Arg
|
|
XM_011514300.1:c.4097T>G
|
XP_011512602.1:p.Leu1366Arg
|
|
XM_011514301.1:c.4034T>G
|
XP_011512603.1:p.Leu1345Arg
|
|
XM_011514302.1:c.3878T>G
|
XP_011512604.1:p.Leu1293Arg
|
|
XM_011514299.2:c.4277T>G
|
XP_011512601.1:p.Leu1426Arg
|
|
XM_011514300.2:c.4097T>G
|
XP_011512602.1:p.Leu1366Arg
|
|
XM_011514302.2:c.3878T>G
|
XP_011512604.1:p.Leu1293Arg
|
|
XM_017010250.1:c.4991T>G
|
XP_016865739.1:p.Leu1664Arg
|
|
XM_017010251.2:c.3809T>G
|
XP_016865740.1:p.Leu1270Arg
|
|
NM_080680.3:c.4991T>G
MANE Select
|
NP_542411.2:p.Leu1664Arg
|
|
NM_080681.3:c.4733T>G
|
NP_542412.2:p.Leu1578Arg
|
|
NM_080679.3:c.4670T>G
|
NP_542410.2:p.Leu1557Arg
|
|