ENST00000350721.9:c.6301G>A
MANE Select
|
ENSP00000343741.4:p.Ala2101Thr
|
|
ENST00000513291.2:n.1485G>A
|
|
|
ENST00000654170.1:n.1144G>A
|
|
|
ENST00000656590.1:c.5091G>A
|
|
|
ENST00000661310.1:c.6109G>A
|
ENSP00000499589.1:p.Ala2037Thr
|
|
ENST00000665483.1:n.156G>A
|
|
|
ENST00000666447.1:n.136G>A
|
|
|
ENST00000666943.1:n.1765G>A
|
|
|
ENST00000350721.8:c.6301G>A
|
ENSP00000343741.4:p.Ala2101Thr
|
|
NM_001184.3:c.6301G>A
|
NP_001175.2:p.Ala2101Thr
|
|
XM_011512924.1:c.6307G>A
|
XP_011511226.1:p.Ala2103Thr
|
|
XM_011512925.1:c.6115G>A
|
XP_011511227.1:p.Ala2039Thr
|
|
XR_924147.1:n.6396G>A
|
|
|
XR_924148.1:n.6396G>A
|
|
|
XR_924149.1:n.6275G>A
|
|
|
NM_001354579.1:c.6109G>A
|
NP_001341508.1:p.Ala2037Thr
|
|
XR_001740179.2:n.6390G>A
|
|
|
XR_001740180.2:n.6444G>A
|
|
|
XR_001740181.2:n.6323G>A
|
|
|
XR_001740182.1:n.6275G>A
|
|
|
XR_002959543.1:n.6500G>A
|
|
|
XR_924148.2:n.6396G>A
|
|
|
NM_001184.4:c.6301G>A
MANE Select
|
NP_001175.2:p.Ala2101Thr
|
|
NM_001354579.2:c.6109G>A
|
NP_001341508.1:p.Ala2037Thr
|
|