|
ENST00000562955.2:c.1496G>T
|
ENSP00000457168.1:p.Ser499Ile
|
|
|
ENST00000634258.3:c.1496G>T
MANE Select
|
ENSP00000489255.1:p.Ser499Ile
|
|
|
ENST00000639852.1:c.1162G>T
|
ENSP00000492385.1:n.1162G>T
|
|
|
ENST00000470139.1:n.227G>T
|
|
|
|
ENST00000562955.1:c.1496G>T
|
ENSP00000457168.1:p.Ser499Ile
|
|
|
ENST00000634258.1:c.1496G>T
|
ENSP00000489255.1:p.Ser499Ile
|
|
|
NM_015284.3:c.1496G>T
|
NP_056099.3:p.Ser499Ile
|
|
|
XM_005270686.2:c.1559G>T
|
XP_005270743.1:p.Ser520Ile
|
|
|
XM_006710501.2:c.1496G>T
|
XP_006710564.1:p.Ser499Ile
|
|
|
XM_011541103.1:c.1613G>T
|
XP_011539405.1:p.Ser538Ile
|
|
|
XM_011541104.1:c.1442G>T
|
XP_011539406.1:p.Ser481Ile
|
|
|
XM_011541105.1:c.1439G>T
|
XP_011539407.1:p.Ser480Ile
|
|
|
XM_011541106.1:c.1439G>T
|
XP_011539408.1:p.Ser480Ile
|
|
|
XM_011541107.1:c.1040G>T
|
XP_011539409.1:p.Ser347Ile
|
|
|
NM_001365999.1:c.1496G>T
MANE Select
|
NP_001352928.1:p.Ser499Ile
|
|
|
XM_005270686.3:c.1559G>T
|
XP_005270743.1:p.Ser520Ile
|
|
|
XM_011541106.3:c.1439G>T
|
XP_011539408.1:p.Ser480Ile
|
|
|
XM_011541107.2:c.1040G>T
|
XP_011539409.1:p.Ser347Ile
|
|
|
XM_017000819.1:c.1559G>T
|
XP_016856308.1:p.Ser520Ile
|
|
|
XM_017000820.1:c.1388G>T
|
XP_016856309.1:p.Ser463Ile
|
|
|
XM_017000821.1:c.188G>T
|
XP_016856310.1:p.Ser63Ile
|
|
|
XR_001737075.1:n.1642G>T
|
|
|
|
XR_001737076.1:n.1644G>T
|
|
|
|
XR_001737077.1:n.1644G>T
|
|
|
|
XR_002956151.1:n.1642G>T
|
|
|
|
NM_015284.4:c.1496G>T
|
NP_056099.3:p.Ser499Ile
|
|
