ENST00000419884.6:c.609A=
|
|
|
ENST00000681993.1:n.1531A=
|
|
|
ENST00000682154.1:n.1413A=
|
|
|
ENST00000682303.1:c.*3690A=
|
ENSP00000508325.1:n.*3690A=
|
|
ENST00000682308.1:c.3904A=
|
ENSP00000507056.1:p.Ser1302=
|
|
ENST00000682434.1:n.3534A=
|
|
|
ENST00000682480.1:c.3997A=
|
ENSP00000508344.1:p.Ser1333=
|
|
ENST00000682546.1:c.3976A=
|
ENSP00000508188.1:p.Ser1326=
|
|
ENST00000682585.1:c.*107A=
|
ENSP00000506885.1:n.*107A=
|
|
ENST00000682607.1:c.2722A=
|
|
|
ENST00000682612.1:c.752+2083A=
|
|
|
ENST00000682696.1:c.79A=
|
ENSP00000508411.1:p.Ser27=
|
|
ENST00000682779.1:c.3970A=
|
ENSP00000507947.1:p.Ser1324=
|
|
ENST00000682885.1:c.3934A=
|
ENSP00000508036.1:p.Ser1312=
|
|
ENST00000682933.1:n.4179A=
|
|
|
ENST00000683002.1:c.831A=
|
|
|
ENST00000683072.1:n.4563A=
|
|
|
ENST00000683080.1:n.1598A=
|
|
|
ENST00000683096.1:n.2420A=
|
|
|
ENST00000683125.1:c.4087A=
|
ENSP00000507939.1:p.Ser1363=
|
|
ENST00000683213.1:c.3982A=
|
ENSP00000507751.1:p.Ser1328=
|
|
ENST00000683220.1:c.4009A=
|
ENSP00000507151.1:p.Ser1337=
|
|
ENST00000683329.1:n.4782A=
|
|
|
ENST00000683346.1:c.*3854A=
|
ENSP00000507458.1:n.*3854A=
|
|
ENST00000683409.1:n.2511A=
|
|
|
ENST00000683459.1:n.4566A=
|
|
|
ENST00000683590.1:c.3652A=
|
ENSP00000506820.1:p.Ser1218=
|
|
ENST00000683623.1:c.3886A=
|
ENSP00000507702.1:p.Ser1296=
|
|
ENST00000683796.1:c.*3776A=
|
ENSP00000508221.1:n.*3776A=
|
|
ENST00000683833.1:c.3895A=
|
ENSP00000506852.1:p.Ser1299=
|
|
ENST00000683994.1:c.*92A=
|
ENSP00000507181.1:n.*92A=
|
|
ENST00000684290.1:c.*1440A=
|
ENSP00000507243.1:n.*1440A=
|
|
ENST00000684306.1:c.*3892A=
|
ENSP00000508384.1:n.*3892A=
|
|
ENST00000684383.1:c.*3617A=
|
ENSP00000506863.1:n.*3617A=
|
|
ENST00000684418.1:n.5160A=
|
|
|
ENST00000684433.1:n.363A=
|
|
|
ENST00000684454.1:n.7843A=
|
|
|
ENST00000684619.1:c.*3851A=
|
ENSP00000508088.1:n.*3851A=
|
|
ENST00000684743.1:n.6724A=
|
|
|
ENST00000260665.12:c.3979A=
MANE Select
|
ENSP00000260665.7:p.Ser1327=
|
|
ENST00000260665.11:c.3979A=
|
ENSP00000260665.7:p.Ser1327=
|
|
ENST00000419884.5:c.220A=
|
ENSP00000414207.1:p.Ser74=
|
|
ENST00000463456.5:n.3022A=
|
|
|
NM_133259.3:c.3979A=
|
NP_573566.2:p.Ser1327=
|
|
XM_006711915.2:c.3901A=
|
XP_006711978.1:p.Ser1301=
|
|
XM_011532473.1:c.3904A=
|
XP_011530775.1:p.Ser1302=
|
|
XM_011532474.1:c.3979A=
|
XP_011530776.1:p.Ser1327=
|
|
XM_017003117.1:c.3826A=
|
XP_016858606.1:p.Ser1276=
|
|
XR_002958896.1:n.4021A=
|
|
|
NM_133259.4:c.3979A=
MANE Select
|
NP_573566.2:p.Ser1327=
|
|