ENST00000683572.1:n.740T>G
|
|
|
ENST00000341947.7:c.4934T>G
MANE Select
|
ENSP00000339915.2:p.Val1645Gly
|
|
ENST00000341947.6:c.4934T>G
|
ENSP00000339915.2:p.Val1645Gly
|
|
ENST00000361917.5:c.4613T>G
|
ENSP00000355123.1:p.Val1538Gly
|
|
ENST00000374708.8:c.4676T>G
|
ENSP00000363840.4:p.Val1559Gly
|
|
ENST00000477772.1:n.724T>G
|
|
|
NM_080679.2:c.4613T>G
|
NP_542410.2:p.Val1538Gly
|
|
NM_080680.2:c.4934T>G
|
NP_542411.2:p.Val1645Gly
|
|
NM_080681.2:c.4676T>G
|
NP_542412.2:p.Val1559Gly
|
|
XM_011514298.1:c.4088T>G
|
XP_011512600.1:p.Val1363Gly
|
|
XM_011514299.1:c.4220T>G
|
XP_011512601.1:p.Val1407Gly
|
|
XM_011514300.1:c.4040T>G
|
XP_011512602.1:p.Val1347Gly
|
|
XM_011514301.1:c.3977T>G
|
XP_011512603.1:p.Val1326Gly
|
|
XM_011514302.1:c.3821T>G
|
XP_011512604.1:p.Val1274Gly
|
|
XM_011514299.2:c.4220T>G
|
XP_011512601.1:p.Val1407Gly
|
|
XM_011514300.2:c.4040T>G
|
XP_011512602.1:p.Val1347Gly
|
|
XM_011514302.2:c.3821T>G
|
XP_011512604.1:p.Val1274Gly
|
|
XM_017010250.1:c.4934T>G
|
XP_016865739.1:p.Val1645Gly
|
|
XM_017010251.2:c.3752T>G
|
XP_016865740.1:p.Val1251Gly
|
|
NM_080680.3:c.4934T>G
MANE Select
|
NP_542411.2:p.Val1645Gly
|
|
NM_080681.3:c.4676T>G
|
NP_542412.2:p.Val1559Gly
|
|
NM_080679.3:c.4613T>G
|
NP_542410.2:p.Val1538Gly
|
|