|
NM_000755.5:c.1811C>T
MANE Select
|
NP_000746.3:p.Ala604Val
|
|
ENST00000318080.7:c.1811C>T
MANE Select
|
ENSP00000315013.2:p.Ala604Val
|
|
NM_000755.3:c.1811C>T
|
NP_000746.2:p.Ala604Val
|
|
NM_000755.4:c.1811C>T
|
NP_000746.2:p.Ala604Val
|
|
NM_001257363.1:c.1748C>T
|
NP_001244292.1:p.Ala583Val
|
|
NM_001257363.2:c.1748C>T
|
NP_001244292.1:p.Ala583Val
|
|
NM_001257363.3:c.1748C>T
|
NP_001244292.2:p.Ala583Val
|
|
NM_001346546.1:c.1814C>T
|
NP_001333475.1:p.Ala605Val
|
|
NM_001346546.2:c.1814C>T
|
NP_001333475.2:p.Ala605Val
|
|
NM_001346547.1:c.1739C>T
|
NP_001333476.1:p.Ala580Val
|
|
NM_001346547.2:c.1739C>T
|
NP_001333476.2:p.Ala580Val
|
|
NM_001346548.1:c.1676C>T
|
NP_001333477.1:p.Ala559Val
|
|
NM_001346548.2:c.1676C>T
|
NP_001333477.2:p.Ala559Val
|
|
NM_001346549.1:c.1691C>T
|
NP_001333478.1:p.Ala564Val
|
|
NM_001346549.2:c.1691C>T
|
NP_001333478.2:p.Ala564Val
|
|
NM_004003.3:c.1748C>T
|
NP_003994.2:p.Ala583Val
|
|
NM_004003.4:c.1748C>T
|
NP_003994.3:p.Ala583Val
|
|
ENST00000318080.6:c.1811C>T
|
ENSP00000315013.2:p.Ala604Val
|
|
ENST00000455396.1:c.534C>T
|
|
|
ENST00000455396.2:c.1691C>T
|
ENSP00000395458.2:p.Ala564Val
|
|
ENST00000458362.5:c.*1787C>T
|
ENSP00000400367.1:n.*1787C>T
|
|
ENST00000467343.1:n.388C>T
|
|
|
ENST00000679520.1:c.*1863C>T
|
ENSP00000505259.1:n.*1863C>T
|
|
ENST00000679716.1:n.3805C>T
|
|
|
ENST00000680093.1:c.*997C>T
|
ENSP00000506286.1:n.*997C>T
|
|
ENST00000680117.1:c.1695C>T
|
ENSP00000505542.1:p.Gly565=
|
|
ENST00000680523.1:n.2793C>T
|
|
|
ENST00000681040.1:c.*1715C>T
|
ENSP00000506678.1:n.*1715C>T
|
|
ENST00000681118.1:n.3277C>T
|
|
|
ENST00000681325.1:c.1586C>T
|
ENSP00000506574.1:p.Ala529Val
|
|
ENST00000681622.1:c.*2067C>T
|
ENSP00000505897.1:n.*2067C>T
|
|
ENST00000681627.1:c.1739C>T
|
ENSP00000506267.1:p.Ala580Val
|
|
ENST00000681689.1:c.*1742C>T
|
ENSP00000505435.1:n.*1742C>T
|
|
ENST00000681911.1:c.*1846C>T
|
ENSP00000506533.1:n.*1846C>T
|
|
XM_005251706.2:c.1814C>T
|
XP_005251763.1:p.Ala605Val
|
|
XM_005251708.2:c.1748C>T
|
XP_005251765.1:p.Ala583Val
|
|
XM_005251708.4:c.1748C>T
|
XP_005251765.1:p.Ala583Val
|
|
XM_017014275.1:c.1814C>T
|
XP_016869764.1:p.Ala605Val
|
|
XM_024447414.1:c.1799C>T
|
XP_024303182.1:p.Ala600Val
|
