ENST00000419884.6:c.200T=
|
|
|
ENST00000472420.6:n.848T=
|
|
|
ENST00000483489.2:n.200T=
|
|
|
ENST00000681993.1:n.1321T=
|
|
|
ENST00000682303.1:c.*3555T=
|
ENSP00000508325.1:n.*3555T=
|
|
ENST00000682308.1:c.3769T=
|
ENSP00000507056.1:p.Phe1257=
|
|
ENST00000682434.1:n.1320T=
|
|
|
ENST00000682480.1:c.3787T=
|
ENSP00000508344.1:p.Phe1263=
|
|
ENST00000682546.1:c.3766T=
|
ENSP00000508188.1:p.Phe1256=
|
|
ENST00000682585.1:c.3769T=
|
ENSP00000506885.1:p.Phe1257=
|
|
ENST00000682595.1:n.4353T=
|
|
|
ENST00000682607.1:c.2187T=
|
|
|
ENST00000682612.1:c.621T=
|
|
|
ENST00000682779.1:c.3760T=
|
ENSP00000507947.1:p.Phe1254=
|
|
ENST00000682845.1:n.2871T=
|
|
|
ENST00000682885.1:c.3724T=
|
ENSP00000508036.1:p.Phe1242=
|
|
ENST00000682933.1:n.3843T=
|
|
|
ENST00000683002.1:c.621T=
|
|
|
ENST00000683072.1:n.4353T=
|
|
|
ENST00000683080.1:n.1388T=
|
|
|
ENST00000683125.1:c.3877T=
|
ENSP00000507939.1:p.Phe1293=
|
|
ENST00000683213.1:c.3772T=
|
ENSP00000507751.1:p.Phe1258=
|
|
ENST00000683220.1:c.3799T=
|
ENSP00000507151.1:p.Phe1267=
|
|
ENST00000683329.1:n.4572T=
|
|
|
ENST00000683346.1:c.*3644T=
|
ENSP00000507458.1:n.*3644T=
|
|
ENST00000683409.1:n.2376T=
|
|
|
ENST00000683459.1:n.4356T=
|
|
|
ENST00000683528.1:c.697T=
|
|
|
ENST00000683590.1:c.3517T=
|
ENSP00000506820.1:p.Phe1173=
|
|
ENST00000683623.1:c.3676T=
|
ENSP00000507702.1:p.Phe1226=
|
|
ENST00000683645.1:n.4320T=
|
|
|
ENST00000683796.1:c.*3641T=
|
ENSP00000508221.1:n.*3641T=
|
|
ENST00000683802.1:n.6694T=
|
|
|
ENST00000683833.1:c.3760T=
|
ENSP00000506852.1:p.Phe1254=
|
|
ENST00000683994.1:c.3769T=
|
ENSP00000507181.1:p.Phe1257=
|
|
ENST00000684290.1:c.*1305T=
|
ENSP00000507243.1:n.*1305T=
|
|
ENST00000684306.1:c.*3682T=
|
ENSP00000508384.1:n.*3682T=
|
|
ENST00000684341.1:n.3789T=
|
|
|
ENST00000684383.1:c.*3407T=
|
ENSP00000506863.1:n.*3407T=
|
|
ENST00000684418.1:n.4950T=
|
|
|
ENST00000684433.1:n.153T=
|
|
|
ENST00000684454.1:n.3119T=
|
|
|
ENST00000684619.1:c.*3641T=
|
ENSP00000508088.1:n.*3641T=
|
|
ENST00000684743.1:n.6514T=
|
|
|
ENST00000260665.12:c.3769T=
MANE Select
|
ENSP00000260665.7:p.Phe1257=
|
|
ENST00000260665.11:c.3769T=
|
ENSP00000260665.7:p.Phe1257=
|
|
ENST00000419884.5:c.10T=
|
ENSP00000414207.1:p.Phe4=
|
|
ENST00000463456.5:n.2812T=
|
|
|
ENST00000472420.5:n.166T=
|
|
|
ENST00000483489.1:n.243T=
|
|
|
NM_133259.3:c.3769T=
|
NP_573566.2:p.Phe1257=
|
|
XM_006711915.2:c.3691T=
|
XP_006711978.1:p.Phe1231=
|
|
XM_011532473.1:c.3769T=
|
XP_011530775.1:p.Phe1257=
|
|
XM_011532474.1:c.3769T=
|
XP_011530776.1:p.Phe1257=
|
|
XM_017003117.1:c.3691T=
|
XP_016858606.1:p.Phe1231=
|
|
XR_002958896.1:n.3811T=
|
|
|
NM_133259.4:c.3769T=
MANE Select
|
NP_573566.2:p.Phe1257=
|
|