ENST00000683572.1:n.661G>T
|
|
|
ENST00000341947.7:c.4855G>T
MANE Select
|
ENSP00000339915.2:p.Val1619Phe
|
|
ENST00000341947.6:c.4855G>T
|
ENSP00000339915.2:p.Val1619Phe
|
|
ENST00000361917.5:c.4534G>T
|
ENSP00000355123.1:p.Val1512Phe
|
|
ENST00000374708.8:c.4597G>T
|
ENSP00000363840.4:p.Val1533Phe
|
|
ENST00000477772.1:n.645G>T
|
|
|
NM_080679.2:c.4534G>T
|
NP_542410.2:p.Val1512Phe
|
|
NM_080680.2:c.4855G>T
|
NP_542411.2:p.Val1619Phe
|
|
NM_080681.2:c.4597G>T
|
NP_542412.2:p.Val1533Phe
|
|
XM_011514298.1:c.4009G>T
|
XP_011512600.1:p.Val1337Phe
|
|
XM_011514299.1:c.4141G>T
|
XP_011512601.1:p.Val1381Phe
|
|
XM_011514300.1:c.3961G>T
|
XP_011512602.1:p.Val1321Phe
|
|
XM_011514301.1:c.3898G>T
|
XP_011512603.1:p.Val1300Phe
|
|
XM_011514302.1:c.3742G>T
|
XP_011512604.1:p.Val1248Phe
|
|
XM_011514299.2:c.4141G>T
|
XP_011512601.1:p.Val1381Phe
|
|
XM_011514300.2:c.3961G>T
|
XP_011512602.1:p.Val1321Phe
|
|
XM_011514302.2:c.3742G>T
|
XP_011512604.1:p.Val1248Phe
|
|
XM_017010250.1:c.4855G>T
|
XP_016865739.1:p.Val1619Phe
|
|
XM_017010251.2:c.3673G>T
|
XP_016865740.1:p.Val1225Phe
|
|
NM_080680.3:c.4855G>T
MANE Select
|
NP_542411.2:p.Val1619Phe
|
|
NM_080681.3:c.4597G>T
|
NP_542412.2:p.Val1533Phe
|
|
NM_080679.3:c.4534G>T
|
NP_542410.2:p.Val1512Phe
|
|