ENST00000472420.6:n.409C>G
|
|
|
ENST00000681993.1:n.882C>G
|
|
|
ENST00000682295.1:c.485C>G
|
ENSP00000507499.1:n.485C>G
|
|
ENST00000682303.1:c.*3116C>G
|
ENSP00000508325.1:n.*3116C>G
|
|
ENST00000682308.1:c.3330C>G
|
ENSP00000507056.1:p.Leu1110=
|
|
ENST00000682480.1:c.3348C>G
|
ENSP00000508344.1:p.Leu1116=
|
|
ENST00000682546.1:c.3327C>G
|
ENSP00000508188.1:p.Leu1109=
|
|
ENST00000682585.1:c.3330C>G
|
ENSP00000506885.1:p.Leu1110=
|
|
ENST00000682595.1:n.3914C>G
|
|
|
ENST00000682607.1:c.1748C>G
|
|
|
ENST00000682612.1:c.182C>G
|
|
|
ENST00000682779.1:c.3321C>G
|
ENSP00000507947.1:p.Leu1107=
|
|
ENST00000682845.1:n.2432C>G
|
|
|
ENST00000682885.1:c.3285C>G
|
ENSP00000508036.1:p.Leu1095=
|
|
ENST00000682933.1:n.3404C>G
|
|
|
ENST00000683002.1:c.182C>G
|
|
|
ENST00000683072.1:n.3914C>G
|
|
|
ENST00000683080.1:n.949C>G
|
|
|
ENST00000683125.1:c.3438C>G
|
ENSP00000507939.1:p.Leu1146=
|
|
ENST00000683213.1:c.3333C>G
|
ENSP00000507751.1:p.Leu1111=
|
|
ENST00000683220.1:c.3360C>G
|
ENSP00000507151.1:p.Leu1120=
|
|
ENST00000683329.1:n.4133C>G
|
|
|
ENST00000683346.1:c.*3205C>G
|
ENSP00000507458.1:n.*3205C>G
|
|
ENST00000683409.1:n.1937C>G
|
|
|
ENST00000683459.1:n.3917C>G
|
|
|
ENST00000683528.1:c.182C>G
|
|
|
ENST00000683590.1:c.3078C>G
|
ENSP00000506820.1:p.Leu1026=
|
|
ENST00000683623.1:c.3237C>G
|
ENSP00000507702.1:p.Leu1079=
|
|
ENST00000683645.1:n.3881C>G
|
|
|
ENST00000683796.1:c.*3202C>G
|
ENSP00000508221.1:n.*3202C>G
|
|
ENST00000683802.1:n.6255C>G
|
|
|
ENST00000683833.1:c.3321C>G
|
ENSP00000506852.1:p.Leu1107=
|
|
ENST00000683994.1:c.3330C>G
|
ENSP00000507181.1:p.Leu1110=
|
|
ENST00000684290.1:c.*866C>G
|
ENSP00000507243.1:n.*866C>G
|
|
ENST00000684306.1:c.*3243C>G
|
ENSP00000508384.1:n.*3243C>G
|
|
ENST00000684341.1:n.3350C>G
|
|
|
ENST00000684383.1:c.*2968C>G
|
ENSP00000506863.1:n.*2968C>G
|
|
ENST00000684418.1:n.4511C>G
|
|
|
ENST00000684454.1:n.2680C>G
|
|
|
ENST00000684619.1:c.*3202C>G
|
ENSP00000508088.1:n.*3202C>G
|
|
ENST00000684743.1:n.4361C>G
|
|
|
ENST00000260665.12:c.3330C>G
MANE Select
|
ENSP00000260665.7:p.Leu1110=
|
|
ENST00000260665.11:c.3330C>G
|
ENSP00000260665.7:p.Leu1110=
|
|
NM_133259.3:c.3330C>G
|
NP_573566.2:p.Leu1110=
|
|
XM_006711915.2:c.3252C>G
|
XP_006711978.1:p.Leu1084=
|
|
XM_011532473.1:c.3330C>G
|
XP_011530775.1:p.Leu1110=
|
|
XM_011532474.1:c.3330C>G
|
XP_011530776.1:p.Leu1110=
|
|
XM_017003117.1:c.3252C>G
|
XP_016858606.1:p.Leu1084=
|
|
XR_002958896.1:n.3372C>G
|
|
|
NM_133259.4:c.3330C>G
MANE Select
|
NP_573566.2:p.Leu1110=
|
|