ENST00000597188.6:c.3312G>T
MANE Select
|
ENSP00000471851.1:p.Ter1104Tyr
|
|
ENST00000270328.8:c.3312G>T
|
ENSP00000270328.4:p.Ter1104Tyr
|
|
ENST00000593913.5:c.*2189G>T
|
ENSP00000469901.1:n.*2189G>T
|
|
ENST00000595838.5:c.1773G>T
|
ENSP00000470501.1:p.Ter591Tyr
|
|
ENST00000597188.5:c.3312G>T
|
ENSP00000471851.1:p.Ter1104Tyr
|
|
NM_001282352.1:c.1773G>T
|
NP_001269281.1:p.Ter591Tyr
|
|
NM_030957.3:c.3312G>T
|
NP_112219.3:p.Ter1104Tyr
|
|
XM_006722917.2:c.2355G>T
|
XP_006722980.1:p.Ter785Tyr
|
|
XM_011528331.1:c.3459G>T
|
XP_011526633.1:p.Ter1153Tyr
|
|
XM_011528332.1:c.3459G>T
|
XP_011526634.1:p.Ter1153Tyr
|
|
XM_011528333.1:c.3459G>T
|
XP_011526635.1:p.Ter1153Tyr
|
|
XM_011528334.1:c.3135G>T
|
XP_011526636.1:p.Ter1045Tyr
|
|
XM_011528335.1:c.2028G>T
|
XP_011526637.1:p.Ter676Tyr
|
|
XM_011528336.1:c.2022G>T
|
XP_011526638.1:p.Ter674Tyr
|
|
XM_006722917.3:c.2355G>T
|
XP_006722980.1:p.Ter785Tyr
|
|
XM_017027338.2:c.3312G>T
|
XP_016882827.1:p.Ter1104Tyr
|
|
XM_017027339.1:c.1881G>T
|
XP_016882828.1:p.Ter627Tyr
|
|
XM_017027340.1:c.1875G>T
|
XP_016882829.1:p.Ter625Tyr
|
|
NM_030957.4:c.3312G>T
MANE Select
|
NP_112219.3:p.Ter1104Tyr
|
|
NM_001282352.2:c.1773G>T
|
NP_001269281.1:p.Ter591Tyr
|
|