ENST00000631006.3:c.436A>G
|
ENSP00000485752.2:p.Ile146Val
|
|
ENST00000695902.1:c.*263A>G
|
ENSP00000512252.1:n.*263A>G
|
|
ENST00000355086.8:c.436A>G
MANE Select
|
ENSP00000347198.3:p.Ile146Val
|
|
ENST00000355086.7:c.436A>G
|
ENSP00000347198.3:p.Ile146Val
|
|
ENST00000537556.1:n.450A>G
|
|
|
ENST00000543397.1:c.316A>G
|
ENSP00000437948.1:p.Ile106Val
|
|
ENST00000631006.2:c.316A>G
|
ENSP00000485752.1:p.Ile106Val
|
|
NM_020762.2:c.436A>G
|
NP_065813.1:p.Ile146Val
|
|
XM_005269042.2:c.436A>G
|
XP_005269099.1:p.Ile146Val
|
|
XM_011538580.1:c.316A>G
|
XP_011536882.1:p.Ile106Val
|
|
XM_011538581.1:c.316A>G
|
XP_011536883.1:p.Ile106Val
|
|
XM_011538582.1:c.13A>G
|
XP_011536884.1:p.Ile5Val
|
|
XM_011538583.1:c.436A>G
|
XP_011536885.1:p.Ile146Val
|
|
XR_945023.1:n.896+2734T>C
|
|
|
NM_001346201.1:c.436A>G
|
NP_001333130.1:p.Ile146Val
|
|
NM_020762.3:c.436A>G
|
NP_065813.1:p.Ile146Val
|
|
XM_011538580.2:c.316A>G
|
XP_011536882.1:p.Ile106Val
|
|
XM_011538581.2:c.316A>G
|
XP_011536883.1:p.Ile106Val
|
|
XM_024449096.1:c.436A>G
|
XP_024304864.1:p.Ile146Val
|
|
XM_024449097.1:c.436A>G
|
XP_024304865.1:p.Ile146Val
|
|
XR_945023.2:n.925+2734T>C
|
|
|
NM_020762.4:c.436A>G
MANE Select
|
NP_065813.1:p.Ile146Val
|
|
NM_001346201.2:c.436A>G
|
NP_001333130.1:p.Ile146Val
|
|