ENST00000553893.6:c.*2200C>T
|
ENSP00000452467.1:n.*2200C>T
|
|
ENST00000554327.6:c.1247C>T
|
|
|
ENST00000557058.2:n.1991C>T
|
|
|
ENST00000557257.2:c.2102C>T
|
ENSP00000450578.2:p.Ala701Val
|
|
ENST00000557555.3:c.2588C>T
|
ENSP00000451039.3:p.Ala863Val
|
|
ENST00000686981.1:c.*2287C>T
|
ENSP00000510795.1:n.*2287C>T
|
|
ENST00000687390.1:n.682C>T
|
|
|
ENST00000691052.1:c.*1060C>T
|
ENSP00000508886.1:n.*1060C>T
|
|
ENST00000691846.1:c.1389C>T
|
|
|
ENST00000691973.1:c.2588C>T
|
ENSP00000509141.1:p.Ala863Val
|
|
ENST00000257879.11:c.2576C>T
MANE Select
|
ENSP00000257879.7:p.Ala859Val
|
|
ENST00000553804.6:c.2588C>T
|
ENSP00000452120.1:p.Ala863Val
|
|
ENST00000257879.10:c.2576C>T
|
ENSP00000257879.6:p.Ala859Val
|
|
ENST00000347027.10:c.2558C>T
|
ENSP00000343009.6:p.Ala853Val
|
|
ENST00000452168.6:c.2297C>T
|
ENSP00000393844.2:p.Ala766Val
|
|
ENST00000553804.5:c.2588C>T
|
ENSP00000452120.1:p.Ala863Val
|
|
ENST00000554327.5:c.641C>T
|
|
|
ENST00000555728.5:c.2708C>T
|
ENSP00000452387.1:p.Ala903Val
|
|
NM_001144996.1:c.2588C>T
|
NP_001138468.1:p.Ala863Val
|
|
NM_001144997.1:c.2297C>T
|
NP_001138469.1:p.Ala766Val
|
|
NM_002206.2:c.2576C>T
|
NP_002197.2:p.Ala859Val
|
|
XM_005268839.1:c.2708C>T
|
XP_005268896.1:p.Ala903Val
|
|
XM_005268840.1:c.2690C>T
|
XP_005268897.1:p.Ala897Val
|
|
XM_005268841.1:c.2708C>T
|
XP_005268898.1:p.Ala903Val
|
|
XM_005268842.1:c.2558C>T
|
XP_005268899.1:p.Ala853Val
|
|
XM_005268844.1:c.2369C>T
|
XP_005268901.1:p.Ala790Val
|
|
XM_005268845.1:c.2237C>T
|
XP_005268902.1:p.Ala746Val
|
|
XM_005268846.1:c.2237C>T
|
XP_005268903.1:p.Ala746Val
|
|
XM_005268847.1:c.2234C>T
|
XP_005268904.1:p.Ala745Val
|
|
XM_005268848.1:c.2234C>T
|
XP_005268905.1:p.Ala745Val
|
|
XM_005268849.1:c.2234C>T
|
XP_005268906.1:p.Ala745Val
|
|
XM_005268850.1:c.2102C>T
|
XP_005268907.1:p.Ala701Val
|
|
XM_011538286.1:c.2369C>T
|
XP_011536588.1:p.Ala790Val
|
|
XM_005268839.2:c.2708C>T
|
XP_005268896.1:p.Ala903Val
|
|
XM_005268840.2:c.2690C>T
|
XP_005268897.1:p.Ala897Val
|
|
XM_005268841.2:c.2708C>T
|
XP_005268898.1:p.Ala903Val
|
|
XM_005268842.2:c.2558C>T
|
XP_005268899.1:p.Ala853Val
|
|
XM_017019265.1:c.2318C>T
|
XP_016874754.1:p.Ala773Val
|
|
NM_001144996.2:c.2588C>T
|
NP_001138468.1:p.Ala863Val
|
|
NM_001367993.1:c.2249C>T
|
NP_001354922.1:p.Ala750Val
|
|
NM_001367994.1:c.1232C>T
|
NP_001354923.1:p.Ala411Val
|
|
NM_001374465.1:c.2558C>T
|
NP_001361394.1:p.Ala853Val
|
|
NM_002206.3:c.2576C>T
MANE Select
|
NP_002197.2:p.Ala859Val
|
|