|
NM_000755.5:c.894C>T
MANE Select
|
NP_000746.3:p.Asp298=
|
|
ENST00000318080.7:c.894C>T
MANE Select
|
ENSP00000315013.2:p.Asp298=
|
|
NM_000755.3:c.894C>T
|
NP_000746.2:p.Asp298=
|
|
NM_000755.4:c.894C>T
|
NP_000746.2:p.Asp298=
|
|
NM_001257363.1:c.831C>T
|
NP_001244292.1:p.Asp277=
|
|
NM_001257363.2:c.831C>T
|
NP_001244292.1:p.Asp277=
|
|
NM_001257363.3:c.831C>T
|
NP_001244292.2:p.Asp277=
|
|
NM_001346546.1:c.897C>T
|
NP_001333475.1:p.Asp299=
|
|
NM_001346546.2:c.897C>T
|
NP_001333475.2:p.Asp299=
|
|
NM_001346547.1:c.894C>T
|
NP_001333476.1:p.Asp298=
|
|
NM_001346547.2:c.894C>T
|
NP_001333476.2:p.Asp298=
|
|
NM_001346548.1:c.831C>T
|
NP_001333477.1:p.Asp277=
|
|
NM_001346548.2:c.831C>T
|
NP_001333477.2:p.Asp277=
|
|
NM_001346549.1:c.774C>T
|
NP_001333478.1:p.Asp258=
|
|
NM_001346549.2:c.774C>T
|
NP_001333478.2:p.Asp258=
|
|
NM_004003.3:c.831C>T
|
NP_003994.2:p.Asp277=
|
|
NM_004003.4:c.831C>T
|
NP_003994.3:p.Asp277=
|
|
ENST00000318080.6:c.894C>T
|
ENSP00000315013.2:p.Asp298=
|
|
ENST00000455396.2:c.774C>T
|
ENSP00000395458.2:p.Asp258=
|
|
ENST00000458362.5:c.*870C>T
|
ENSP00000400367.1:n.*870C>T
|
|
ENST00000679520.1:c.*946C>T
|
ENSP00000505259.1:n.*946C>T
|
|
ENST00000679716.1:n.2888C>T
|
|
|
ENST00000680093.1:c.*80C>T
|
ENSP00000506286.1:n.*80C>T
|
|
ENST00000680117.1:c.894C>T
|
ENSP00000505542.1:p.Asp298=
|
|
ENST00000680523.1:n.1176C>T
|
|
|
ENST00000681040.1:c.*870C>T
|
ENSP00000506678.1:n.*870C>T
|
|
ENST00000681118.1:n.2360C>T
|
|
|
ENST00000681325.1:c.894C>T
|
ENSP00000506574.1:p.Asp298=
|
|
ENST00000681622.1:c.*1150C>T
|
ENSP00000505897.1:n.*1150C>T
|
|
ENST00000681627.1:c.894C>T
|
ENSP00000506267.1:p.Asp298=
|
|
ENST00000681689.1:c.*870C>T
|
ENSP00000505435.1:n.*870C>T
|
|
ENST00000681725.1:c.894C>T
|
ENSP00000505817.1:p.Asp298=
|
|
ENST00000681911.1:c.*929C>T
|
ENSP00000506533.1:n.*929C>T
|
|
XM_005251706.2:c.897C>T
|
XP_005251763.1:p.Asp299=
|
|
XM_005251708.2:c.831C>T
|
XP_005251765.1:p.Asp277=
|
|
XM_005251708.4:c.831C>T
|
XP_005251765.1:p.Asp277=
|
|
XM_017014275.1:c.897C>T
|
XP_016869764.1:p.Asp299=
|
|
XM_024447414.1:c.882C>T
|
XP_024303182.1:p.Asp294=
|
