ENST00000231887.8:c.13A>G
MANE Select
|
ENSP00000231887.3:p.Thr5Ala
|
|
ENST00000231887.7:c.13A>G
|
ENSP00000231887.3:p.Thr5Ala
|
|
ENST00000440662.1:c.13A>G
|
ENSP00000396798.1:p.Thr5Ala
|
|
ENST00000456310.5:c.-399A>G
|
ENSP00000387746.1:n.-399A>G
|
|
ENST00000465178.1:n.228-5493A>G
|
|
|
ENST00000475987.1:n.40A>G
|
|
|
NM_001166415.1:c.-399A>G
|
NP_001159887.1:n.-399A>G
|
|
NM_001966.3:c.13A>G
|
NP_001957.2:p.Thr5Ala
|
|
XM_006713525.1:c.-643A>G
|
XP_006713588.1:n.-643A>G
|
|
XM_011512517.1:c.-214-5493A>G
|
XP_011510819.1:n.-214-5493A>G
|
|
NM_001966.4:c.13A>G
MANE Select
|
NP_001957.2:p.Thr5Ala
|
|
NM_001166415.2:c.-399A>G
|
NP_001159887.1:n.-399A>G
|
|