ENST00000683572.1:n.739G=
|
|
|
ENST00000341947.7:c.4933G=
MANE Select
|
ENSP00000339915.2:p.Val1645=
|
|
ENST00000341947.6:c.4933G=
|
ENSP00000339915.2:p.Val1645=
|
|
ENST00000361917.5:c.4612G=
|
ENSP00000355123.1:p.Val1538=
|
|
ENST00000374708.8:c.4675G=
|
ENSP00000363840.4:p.Val1559=
|
|
ENST00000477772.1:n.723G=
|
|
|
NM_080679.2:c.4612G=
|
NP_542410.2:p.Val1538=
|
|
NM_080680.2:c.4933G=
|
NP_542411.2:p.Val1645=
|
|
NM_080681.2:c.4675G=
|
NP_542412.2:p.Val1559=
|
|
XM_011514298.1:c.4087G=
|
XP_011512600.1:p.Val1363=
|
|
XM_011514299.1:c.4219G=
|
XP_011512601.1:p.Val1407=
|
|
XM_011514300.1:c.4039G=
|
XP_011512602.1:p.Val1347=
|
|
XM_011514301.1:c.3976G=
|
XP_011512603.1:p.Val1326=
|
|
XM_011514302.1:c.3820G=
|
XP_011512604.1:p.Val1274=
|
|
XM_011514299.2:c.4219G=
|
XP_011512601.1:p.Val1407=
|
|
XM_011514300.2:c.4039G=
|
XP_011512602.1:p.Val1347=
|
|
XM_011514302.2:c.3820G=
|
XP_011512604.1:p.Val1274=
|
|
XM_017010250.1:c.4933G=
|
XP_016865739.1:p.Val1645=
|
|
XM_017010251.2:c.3751G=
|
XP_016865740.1:p.Val1251=
|
|
NM_080680.3:c.4933G=
MANE Select
|
NP_542411.2:p.Val1645=
|
|
NM_080681.3:c.4675G=
|
NP_542412.2:p.Val1559=
|
|
NM_080679.3:c.4612G=
|
NP_542410.2:p.Val1538=
|
|