ENST00000361492.9:c.4529G>T
MANE Select
|
ENSP00000354586.5:p.Gly1510Val
|
|
ENST00000452319.6:c.4580G>T
|
ENSP00000390436.1:p.Gly1527Val
|
|
ENST00000341310.10:c.*3628G>T
|
ENSP00000344473.6:n.*3628G>T
|
|
ENST00000361492.8:c.4580G>T
|
ENSP00000354586.4:p.Gly1527Val
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|
ENST00000438299.5:c.*2544-96G>T
|
ENSP00000400593.1:n.*2544-96G>T
|
|
ENST00000445186.5:c.*3679G>T
|
ENSP00000397488.1:n.*3679G>T
|
|
ENST00000452319.5:c.4580G>T
|
ENSP00000390436.1:p.Gly1527Val
|
|
ENST00000452692.5:c.*2493-96G>T
|
ENSP00000403715.1:n.*2493-96G>T
|
|
NM_005270.4:c.4580G>T
|
NP_005261.2:p.Gly1527Val
|
|
XM_006712422.1:c.4529G>T
|
XP_006712485.1:p.Gly1510Val
|
|
XM_011510969.1:c.4562G>T
|
XP_011509271.1:p.Gly1521Val
|
|
XM_011510970.1:c.4439G>T
|
XP_011509272.1:p.Gly1480Val
|
|
XM_011510971.1:c.4385G>T
|
XP_011509273.1:p.Gly1462Val
|
|
XM_011510972.1:c.4385G>T
|
XP_011509274.1:p.Gly1462Val
|
|
XM_011510973.1:c.4205G>T
|
XP_011509275.1:p.Gly1402Val
|
|
XM_011510974.1:c.4154G>T
|
XP_011509276.1:p.Gly1385Val
|
|
XM_006712422.3:c.4529G>T
|
XP_006712485.1:p.Gly1510Val
|
|
XM_011510969.2:c.4832G>T
|
XP_011509271.2:p.Gly1611Val
|
|
XM_011510970.2:c.4439G>T
|
XP_011509272.1:p.Gly1480Val
|
|
XM_011510971.2:c.4385G>T
|
XP_011509273.1:p.Gly1462Val
|
|
XM_011510972.2:c.4481G>T
|
XP_011509274.2:p.Gly1494Val
|
|
XM_011510973.2:c.4205G>T
|
XP_011509275.1:p.Gly1402Val
|
|
XM_011510974.2:c.4154G>T
|
XP_011509276.1:p.Gly1385Val
|
|
XM_017003818.1:c.4781G>T
|
XP_016859307.1:p.Gly1594Val
|
|
XM_024452794.1:c.4580G>T
|
XP_024308562.1:p.Gly1527Val
|
|
XM_024452795.1:c.4580G>T
|
XP_024308563.1:p.Gly1527Val
|
|
NM_001371271.1:c.4580G>T
|
NP_001358200.1:p.Gly1527Val
|
|
NM_001374353.1:c.4529G>T
MANE Select
|
NP_001361282.1:p.Gly1510Val
|
|
NM_001374354.1:c.4154G>T
|
NP_001361283.1:p.Gly1385Val
|
|
NM_005270.5:c.4580G>T
|
NP_005261.2:p.Gly1527Val
|
|