ENST00000350721.9:c.4576A>G
MANE Select
|
ENSP00000343741.4:p.Ile1526Val
|
|
ENST00000653868.1:n.4605A>G
|
|
|
ENST00000656590.1:c.3366A>G
|
|
|
ENST00000661310.1:c.4384A>G
|
ENSP00000499589.1:p.Ile1462Val
|
|
ENST00000666943.1:n.40A>G
|
|
|
ENST00000350721.8:c.4576A>G
|
ENSP00000343741.4:p.Ile1526Val
|
|
NM_001184.3:c.4576A>G
|
NP_001175.2:p.Ile1526Val
|
|
XM_011512924.1:c.4582A>G
|
XP_011511226.1:p.Ile1528Val
|
|
XM_011512925.1:c.4390A>G
|
XP_011511227.1:p.Ile1464Val
|
|
XM_011512926.1:c.4582A>G
|
XP_011511228.1:p.Ile1528Val
|
|
XM_011512927.1:c.4582A>G
|
XP_011511229.1:p.Ile1528Val
|
|
XR_924147.1:n.4671A>G
|
|
|
XR_924148.1:n.4671A>G
|
|
|
XR_924149.1:n.4671A>G
|
|
|
NM_001354579.1:c.4384A>G
|
NP_001341508.1:p.Ile1462Val
|
|
XR_001740179.2:n.4665A>G
|
|
|
XR_001740180.2:n.4671A>G
|
|
|
XR_001740181.2:n.4671A>G
|
|
|
XR_001740182.1:n.4671A>G
|
|
|
XR_002959543.1:n.4671A>G
|
|
|
XR_924148.2:n.4671A>G
|
|
|
NM_001184.4:c.4576A>G
MANE Select
|
NP_001175.2:p.Ile1526Val
|
|
NM_001354579.2:c.4384A>G
|
NP_001341508.1:p.Ile1462Val
|
|