ENST00000350721.9:c.4528A>G
MANE Select
|
ENSP00000343741.4:p.Ile1510Val
|
|
ENST00000653868.1:n.4557A>G
|
|
|
ENST00000656590.1:c.3318A>G
|
|
|
ENST00000661310.1:c.4336A>G
|
ENSP00000499589.1:p.Ile1446Val
|
|
ENST00000350721.8:c.4528A>G
|
ENSP00000343741.4:p.Ile1510Val
|
|
NM_001184.3:c.4528A>G
|
NP_001175.2:p.Ile1510Val
|
|
XM_011512924.1:c.4534A>G
|
XP_011511226.1:p.Ile1512Val
|
|
XM_011512925.1:c.4342A>G
|
XP_011511227.1:p.Ile1448Val
|
|
XM_011512926.1:c.4534A>G
|
XP_011511228.1:p.Ile1512Val
|
|
XM_011512927.1:c.4534A>G
|
XP_011511229.1:p.Ile1512Val
|
|
XR_924147.1:n.4623A>G
|
|
|
XR_924148.1:n.4623A>G
|
|
|
XR_924149.1:n.4623A>G
|
|
|
NM_001354579.1:c.4336A>G
|
NP_001341508.1:p.Ile1446Val
|
|
XR_001740179.2:n.4617A>G
|
|
|
XR_001740180.2:n.4623A>G
|
|
|
XR_001740181.2:n.4623A>G
|
|
|
XR_001740182.1:n.4623A>G
|
|
|
XR_002959543.1:n.4623A>G
|
|
|
XR_924148.2:n.4623A>G
|
|
|
NM_001184.4:c.4528A>G
MANE Select
|
NP_001175.2:p.Ile1510Val
|
|
NM_001354579.2:c.4336A>G
|
NP_001341508.1:p.Ile1446Val
|
|