|
ENST00000419884.6:c.532C>G
|
|
|
|
ENST00000681993.1:n.1454C>G
|
|
|
|
ENST00000682154.1:n.1336C>G
|
|
|
|
ENST00000682303.1:c.*3613C>G
|
ENSP00000508325.1:n.*3613C>G
|
|
|
ENST00000682308.1:c.3827C>G
|
ENSP00000507056.1:p.Ala1276Gly
|
|
|
ENST00000682434.1:n.3457C>G
|
|
|
|
ENST00000682480.1:c.3920C>G
|
ENSP00000508344.1:p.Ala1307Gly
|
|
|
ENST00000682546.1:c.3899C>G
|
ENSP00000508188.1:p.Ala1300Gly
|
|
|
ENST00000682585.1:c.*30C>G
|
ENSP00000506885.1:n.*30C>G
|
|
|
ENST00000682607.1:c.2645C>G
|
|
|
|
ENST00000682612.1:c.752+2006C>G
|
|
|
|
ENST00000682696.1:c.2C>G
|
ENSP00000508411.1:p.Ala1Gly
|
|
|
ENST00000682779.1:c.3893C>G
|
ENSP00000507947.1:p.Ala1298Gly
|
|
|
ENST00000682885.1:c.3857C>G
|
ENSP00000508036.1:p.Ala1286Gly
|
|
|
ENST00000682933.1:n.4102C>G
|
|
|
|
ENST00000683002.1:c.754C>G
|
|
|
|
ENST00000683072.1:n.4486C>G
|
|
|
|
ENST00000683080.1:n.1521C>G
|
|
|
|
ENST00000683096.1:n.2343C>G
|
|
|
|
ENST00000683125.1:c.4010C>G
|
ENSP00000507939.1:p.Ala1337Gly
|
|
|
ENST00000683213.1:c.3905C>G
|
ENSP00000507751.1:p.Ala1302Gly
|
|
|
ENST00000683220.1:c.3932C>G
|
ENSP00000507151.1:p.Ala1311Gly
|
|
|
ENST00000683329.1:n.4705C>G
|
|
|
|
ENST00000683346.1:c.*3777C>G
|
ENSP00000507458.1:n.*3777C>G
|
|
|
ENST00000683409.1:n.2434C>G
|
|
|
|
ENST00000683459.1:n.4489C>G
|
|
|
|
ENST00000683590.1:c.3575C>G
|
ENSP00000506820.1:p.Ala1192Gly
|
|
|
ENST00000683623.1:c.3809C>G
|
ENSP00000507702.1:p.Ala1270Gly
|
|
|
ENST00000683796.1:c.*3699C>G
|
ENSP00000508221.1:n.*3699C>G
|
|
|
ENST00000683833.1:c.3818C>G
|
ENSP00000506852.1:p.Ala1273Gly
|
|
|
ENST00000683994.1:c.*15C>G
|
ENSP00000507181.1:n.*15C>G
|
|
|
ENST00000684290.1:c.*1363C>G
|
ENSP00000507243.1:n.*1363C>G
|
|
|
ENST00000684306.1:c.*3815C>G
|
ENSP00000508384.1:n.*3815C>G
|
|
|
ENST00000684383.1:c.*3540C>G
|
ENSP00000506863.1:n.*3540C>G
|
|
|
ENST00000684418.1:n.5083C>G
|
|
|
|
ENST00000684433.1:n.286C>G
|
|
|
|
ENST00000684454.1:n.7766C>G
|
|
|
|
ENST00000684619.1:c.*3774C>G
|
ENSP00000508088.1:n.*3774C>G
|
|
|
ENST00000684743.1:n.6647C>G
|
|
|
|
ENST00000260665.12:c.3902C>G
MANE Select
|
ENSP00000260665.7:p.Ala1301Gly
|
|
|
ENST00000260665.11:c.3902C>G
|
ENSP00000260665.7:p.Ala1301Gly
|
|
|
ENST00000419884.5:c.143C>G
|
ENSP00000414207.1:p.Ala48Gly
|
|
|
ENST00000463456.5:n.2945C>G
|
|
|
|
NM_133259.3:c.3902C>G
|
NP_573566.2:p.Ala1301Gly
|
|
|
XM_006711915.2:c.3824C>G
|
XP_006711978.1:p.Ala1275Gly
|
|
|
XM_011532473.1:c.3827C>G
|
XP_011530775.1:p.Ala1276Gly
|
|
|
XM_011532474.1:c.3902C>G
|
XP_011530776.1:p.Ala1301Gly
|
|
|
XM_017003117.1:c.3749C>G
|
XP_016858606.1:p.Ala1250Gly
|
|
|
XR_002958896.1:n.3944C>G
|
|
|
|
NM_133259.4:c.3902C>G
MANE Select
|
NP_573566.2:p.Ala1301Gly
|
|
