ENST00000318158.11:c.574G>A
MANE Select
|
ENSP00000313432.6:p.Ala192Thr
|
|
ENST00000318158.10:c.574G>A
|
ENSP00000313432.6:p.Ala192Thr
|
|
ENST00000377824.8:n.611G>A
|
|
|
ENST00000460882.5:n.601G>A
|
|
|
ENST00000480596.5:n.1275G>A
|
|
|
ENST00000482603.1:n.27G>A
|
|
|
ENST00000491488.5:n.279G>A
|
|
|
ENST00000494290.1:c.145G>A
|
ENSP00000432021.1:p.Ala49Thr
|
|
ENST00000497693.1:n.2107G>A
|
|
|
ENST00000607784.1:c.574G>A
|
ENSP00000475569.1:p.Ala192Thr
|
|
NM_012203.1:c.574G>A
|
NP_036335.1:p.Ala192Thr
|
|
XM_005251631.1:c.253G>A
|
XP_005251688.1:p.Ala85Thr
|
|
XM_011518073.1:c.172G>A
|
XP_011516375.1:p.Ala58Thr
|
|
XR_929374.1:n.1019G>A
|
|
|
XM_017015320.2:c.574G>A
|
XP_016870809.1:p.Ala192Thr
|
|
XM_017015321.2:c.574G>A
|
XP_016870810.1:p.Ala192Thr
|
|
XM_017015323.2:c.172G>A
|
XP_016870812.1:p.Ala58Thr
|
|
XM_024447716.1:c.847G>A
|
XP_024303484.1:p.Ala283Thr
|
|
XM_024447717.1:c.847G>A
|
XP_024303485.1:p.Ala283Thr
|
|
XR_002956828.1:n.862G>A
|
|
|
XR_002956829.1:n.862G>A
|
|
|
XR_002956830.1:n.633G>A
|
|
|
XR_002956831.1:n.308G>A
|
|
|
XR_002956832.1:n.993G>A
|
|
|
NM_012203.2:c.574G>A
MANE Select
|
NP_036335.1:p.Ala192Thr
|
|