ENST00000683572.1:n.796C>G
|
|
|
ENST00000341947.7:c.4990C>G
MANE Select
|
ENSP00000339915.2:p.Leu1664Val
|
|
ENST00000341947.6:c.4990C>G
|
ENSP00000339915.2:p.Leu1664Val
|
|
ENST00000361917.5:c.4669C>G
|
ENSP00000355123.1:p.Leu1557Val
|
|
ENST00000374708.8:c.4732C>G
|
ENSP00000363840.4:p.Leu1578Val
|
|
ENST00000477772.1:n.780C>G
|
|
|
NM_080679.2:c.4669C>G
|
NP_542410.2:p.Leu1557Val
|
|
NM_080680.2:c.4990C>G
|
NP_542411.2:p.Leu1664Val
|
|
NM_080681.2:c.4732C>G
|
NP_542412.2:p.Leu1578Val
|
|
XM_011514298.1:c.4144C>G
|
XP_011512600.1:p.Leu1382Val
|
|
XM_011514299.1:c.4276C>G
|
XP_011512601.1:p.Leu1426Val
|
|
XM_011514300.1:c.4096C>G
|
XP_011512602.1:p.Leu1366Val
|
|
XM_011514301.1:c.4033C>G
|
XP_011512603.1:p.Leu1345Val
|
|
XM_011514302.1:c.3877C>G
|
XP_011512604.1:p.Leu1293Val
|
|
XM_011514299.2:c.4276C>G
|
XP_011512601.1:p.Leu1426Val
|
|
XM_011514300.2:c.4096C>G
|
XP_011512602.1:p.Leu1366Val
|
|
XM_011514302.2:c.3877C>G
|
XP_011512604.1:p.Leu1293Val
|
|
XM_017010250.1:c.4990C>G
|
XP_016865739.1:p.Leu1664Val
|
|
XM_017010251.2:c.3808C>G
|
XP_016865740.1:p.Leu1270Val
|
|
NM_080680.3:c.4990C>G
MANE Select
|
NP_542411.2:p.Leu1664Val
|
|
NM_080681.3:c.4732C>G
|
NP_542412.2:p.Leu1578Val
|
|
NM_080679.3:c.4669C>G
|
NP_542410.2:p.Leu1557Val
|
|