ENST00000395762.7:c.1558G>A
MANE Select
|
ENSP00000379111.2:p.Ala520Thr
|
|
ENST00000170630.6:c.1513G>A
|
ENSP00000170630.3:p.Ala505Thr
|
|
ENST00000395762.6:c.1558G>A
|
ENSP00000379111.2:p.Ala520Thr
|
|
ENST00000543915.6:c.1558G>A
|
ENSP00000441667.2:p.Ala520Thr
|
|
ENST00000565352.1:c.230-1193G>A
|
ENSP00000461268.1:n.230-1193G>A
|
|
ENST00000568746.5:c.*1601G>A
|
ENSP00000455714.1:n.*1601G>A
|
|
NM_000418.3:c.1558G>A
|
NP_000409.1:p.Ala520Thr
|
|
NM_001257406.1:c.1558G>A
|
NP_001244335.1:p.Ala520Thr
|
|
NM_001257407.1:c.1513G>A
|
NP_001244336.1:p.Ala505Thr
|
|
NM_001257997.1:c.1078G>A
|
NP_001244926.1:p.Ala360Thr
|
|
XM_005255308.2:c.667G>A
|
XP_005255365.1:p.Ala223Thr
|
|
XM_006721043.1:c.607G>A
|
XP_006721106.1:p.Ala203Thr
|
|
XM_011545825.1:c.1558G>A
|
XP_011544127.1:p.Ala520Thr
|
|
XM_011545826.1:c.1558G>A
|
XP_011544128.1:p.Ala520Thr
|
|
XM_011545827.1:c.1558G>A
|
XP_011544129.1:p.Ala520Thr
|
|
XM_011545828.1:c.1291G>A
|
XP_011544130.1:p.Ala431Thr
|
|
XM_011545829.1:c.1261G>A
|
XP_011544131.1:p.Ala421Thr
|
|
XM_011545830.1:c.1261G>A
|
XP_011544132.1:p.Ala421Thr
|
|
XM_011545831.1:c.1261G>A
|
XP_011544133.1:p.Ala421Thr
|
|
XM_011545832.1:c.1261G>A
|
XP_011544134.1:p.Ala421Thr
|
|
XM_011545833.1:c.1261G>A
|
XP_011544135.1:p.Ala421Thr
|
|
XM_011545834.1:c.1135G>A
|
XP_011544136.1:p.Ala379Thr
|
|
XM_011545826.2:c.1558G>A
|
XP_011544128.1:p.Ala520Thr
|
|
XM_011545827.2:c.1558G>A
|
XP_011544129.1:p.Ala520Thr
|
|
XM_011545828.2:c.1291G>A
|
XP_011544130.1:p.Ala431Thr
|
|
XM_011545830.2:c.1261G>A
|
XP_011544132.1:p.Ala421Thr
|
|
XM_011545833.2:c.1261G>A
|
XP_011544135.1:p.Ala421Thr
|
|
XM_011545834.2:c.1135G>A
|
XP_011544136.1:p.Ala379Thr
|
|
NM_000418.4:c.1558G>A
MANE Select
|
NP_000409.1:p.Ala520Thr
|
|
NM_001257406.2:c.1558G>A
|
NP_001244335.1:p.Ala520Thr
|
|
NM_001257407.2:c.1513G>A
|
NP_001244336.1:p.Ala505Thr
|
|
NM_001257997.2:c.1078G>A
|
NP_001244926.1:p.Ala360Thr
|
|