ENST00000683572.1:n.802C>G
|
|
|
ENST00000341947.7:c.4996C>G
MANE Select
|
ENSP00000339915.2:p.Leu1666Val
|
|
ENST00000341947.6:c.4996C>G
|
ENSP00000339915.2:p.Leu1666Val
|
|
ENST00000361917.5:c.4675C>G
|
ENSP00000355123.1:p.Leu1559Val
|
|
ENST00000374708.8:c.4738C>G
|
ENSP00000363840.4:p.Leu1580Val
|
|
ENST00000477772.1:n.786C>G
|
|
|
NM_080679.2:c.4675C>G
|
NP_542410.2:p.Leu1559Val
|
|
NM_080680.2:c.4996C>G
|
NP_542411.2:p.Leu1666Val
|
|
NM_080681.2:c.4738C>G
|
NP_542412.2:p.Leu1580Val
|
|
XM_011514298.1:c.4150C>G
|
XP_011512600.1:p.Leu1384Val
|
|
XM_011514299.1:c.4282C>G
|
XP_011512601.1:p.Leu1428Val
|
|
XM_011514300.1:c.4102C>G
|
XP_011512602.1:p.Leu1368Val
|
|
XM_011514301.1:c.4039C>G
|
XP_011512603.1:p.Leu1347Val
|
|
XM_011514302.1:c.3883C>G
|
XP_011512604.1:p.Leu1295Val
|
|
XM_011514299.2:c.4282C>G
|
XP_011512601.1:p.Leu1428Val
|
|
XM_011514300.2:c.4102C>G
|
XP_011512602.1:p.Leu1368Val
|
|
XM_011514302.2:c.3883C>G
|
XP_011512604.1:p.Leu1295Val
|
|
XM_017010250.1:c.4996C>G
|
XP_016865739.1:p.Leu1666Val
|
|
XM_017010251.2:c.3814C>G
|
XP_016865740.1:p.Leu1272Val
|
|
NM_080680.3:c.4996C>G
MANE Select
|
NP_542411.2:p.Leu1666Val
|
|
NM_080681.3:c.4738C>G
|
NP_542412.2:p.Leu1580Val
|
|
NM_080679.3:c.4675C>G
|
NP_542410.2:p.Leu1559Val
|
|