ENST00000472420.6:n.412C>T
|
|
|
ENST00000681993.1:n.885C>T
|
|
|
ENST00000682295.1:c.488C>T
|
ENSP00000507499.1:n.488C>T
|
|
ENST00000682303.1:c.*3119C>T
|
ENSP00000508325.1:n.*3119C>T
|
|
ENST00000682308.1:c.3333C>T
|
ENSP00000507056.1:p.Ile1111=
|
|
ENST00000682480.1:c.3351C>T
|
ENSP00000508344.1:p.Ile1117=
|
|
ENST00000682546.1:c.3330C>T
|
ENSP00000508188.1:p.Ile1110=
|
|
ENST00000682585.1:c.3333C>T
|
ENSP00000506885.1:p.Ile1111=
|
|
ENST00000682595.1:n.3917C>T
|
|
|
ENST00000682607.1:c.1751C>T
|
|
|
ENST00000682612.1:c.185C>T
|
|
|
ENST00000682779.1:c.3324C>T
|
ENSP00000507947.1:p.Ile1108=
|
|
ENST00000682845.1:n.2435C>T
|
|
|
ENST00000682885.1:c.3288C>T
|
ENSP00000508036.1:p.Ile1096=
|
|
ENST00000682933.1:n.3407C>T
|
|
|
ENST00000683002.1:c.185C>T
|
|
|
ENST00000683072.1:n.3917C>T
|
|
|
ENST00000683080.1:n.952C>T
|
|
|
ENST00000683125.1:c.3441C>T
|
ENSP00000507939.1:p.Ile1147=
|
|
ENST00000683213.1:c.3336C>T
|
ENSP00000507751.1:p.Ile1112=
|
|
ENST00000683220.1:c.3363C>T
|
ENSP00000507151.1:p.Ile1121=
|
|
ENST00000683329.1:n.4136C>T
|
|
|
ENST00000683346.1:c.*3208C>T
|
ENSP00000507458.1:n.*3208C>T
|
|
ENST00000683409.1:n.1940C>T
|
|
|
ENST00000683459.1:n.3920C>T
|
|
|
ENST00000683528.1:c.185C>T
|
|
|
ENST00000683590.1:c.3081C>T
|
ENSP00000506820.1:p.Ile1027=
|
|
ENST00000683623.1:c.3240C>T
|
ENSP00000507702.1:p.Ile1080=
|
|
ENST00000683645.1:n.3884C>T
|
|
|
ENST00000683796.1:c.*3205C>T
|
ENSP00000508221.1:n.*3205C>T
|
|
ENST00000683802.1:n.6258C>T
|
|
|
ENST00000683833.1:c.3324C>T
|
ENSP00000506852.1:p.Ile1108=
|
|
ENST00000683994.1:c.3333C>T
|
ENSP00000507181.1:p.Ile1111=
|
|
ENST00000684290.1:c.*869C>T
|
ENSP00000507243.1:n.*869C>T
|
|
ENST00000684306.1:c.*3246C>T
|
ENSP00000508384.1:n.*3246C>T
|
|
ENST00000684341.1:n.3353C>T
|
|
|
ENST00000684383.1:c.*2971C>T
|
ENSP00000506863.1:n.*2971C>T
|
|
ENST00000684418.1:n.4514C>T
|
|
|
ENST00000684454.1:n.2683C>T
|
|
|
ENST00000684619.1:c.*3205C>T
|
ENSP00000508088.1:n.*3205C>T
|
|
ENST00000684743.1:n.4364C>T
|
|
|
ENST00000260665.12:c.3333C>T
MANE Select
|
ENSP00000260665.7:p.Ile1111=
|
|
ENST00000260665.11:c.3333C>T
|
ENSP00000260665.7:p.Ile1111=
|
|
NM_133259.3:c.3333C>T
|
NP_573566.2:p.Ile1111=
|
|
XM_006711915.2:c.3255C>T
|
XP_006711978.1:p.Ile1085=
|
|
XM_011532473.1:c.3333C>T
|
XP_011530775.1:p.Ile1111=
|
|
XM_011532474.1:c.3333C>T
|
XP_011530776.1:p.Ile1111=
|
|
XM_017003117.1:c.3255C>T
|
XP_016858606.1:p.Ile1085=
|
|
XR_002958896.1:n.3375C>T
|
|
|
NM_133259.4:c.3333C>T
MANE Select
|
NP_573566.2:p.Ile1111=
|
|