|
ENST00000682071.1:c.1120C>T
|
ENSP00000508133.1:p.Gln374Ter
|
|
|
ENST00000682899.1:n.1696C>T
|
|
|
|
ENST00000682924.1:c.1338C>T
|
ENSP00000508187.1:p.Phe446=
|
|
|
ENST00000683985.1:n.1696C>T
|
|
|
|
ENST00000684165.1:n.1696C>T
|
|
|
|
ENST00000684237.1:c.1360C>T
|
ENSP00000507277.1:p.Gln454Ter
|
|
|
ENST00000684292.1:n.1696C>T
|
|
|
|
ENST00000288447.9:c.1465C>T
|
ENSP00000288447.4:p.Gln489Ter
|
|
|
ENST00000357033.9:c.1489C>T
MANE Select
|
ENSP00000354923.3:p.Gln497Ter
|
|
|
ENST00000288447.8:c.1465C>T
|
ENSP00000288447.4:p.Gln489Ter
|
|
|
ENST00000357033.8:c.1489C>T
|
ENSP00000354923.3:p.Gln497Ter
|
|
|
ENST00000378677.6:c.1477C>T
|
ENSP00000367948.2:p.Gln493Ter
|
|
|
ENST00000420596.5:c.94-230671C>T
|
ENSP00000399897.1:n.94-230671C>T
|
|
|
ENST00000447523.1:c.247-22024C>T
|
ENSP00000395904.1:n.247-22024C>T
|
|
|
ENST00000448370.5:c.94-231160C>T
|
ENSP00000388559.1:n.94-231160C>T
|
|
|
ENST00000480751.1:n.87-22024C>T
|
|
|
|
ENST00000488902.5:n.336-378807C>T
|
|
|
|
ENST00000619831.4:c.1477C>T
|
ENSP00000479270.1:p.Gln493Ter
|
|
|
ENST00000620040.4:c.1489C>T
|
ENSP00000478150.1:p.Gln497Ter
|
|
|
NM_000109.3:c.1465C>T
|
NP_000100.2:p.Gln489Ter
|
|
|
NM_004006.2:c.1489C>T , LRG_199t1:c.1489C>T
|
NP_003997.1:p.Gln497Ter
|
|
|
NM_004009.3:c.1477C>T
|
NP_004000.1:p.Gln493Ter
|
|
|
NM_004010.3:c.1120C>T
|
NP_004001.1:p.Gln374Ter
|
|
|
XM_006724468.2:c.1489C>T
|
XP_006724531.1:p.Gln497Ter
|
|
|
XM_006724469.2:c.1465C>T
|
XP_006724532.1:p.Gln489Ter
|
|
|
XM_006724470.2:c.1489C>T
|
XP_006724533.1:p.Gln497Ter
|
|
|
XM_006724471.2:c.1489C>T
|
XP_006724534.1:p.Gln497Ter
|
|
|
XM_006724472.2:c.1360C>T
|
XP_006724535.1:p.Gln454Ter
|
|
|
XM_006724473.2:c.1489C>T
|
XP_006724536.1:p.Gln497Ter
|
|
|
XM_006724474.2:c.1489C>T
|
XP_006724537.1:p.Gln497Ter
|
|
|
XM_006724475.2:c.1489C>T
|
XP_006724538.1:p.Gln497Ter
|
|
|
XM_011545467.1:c.1489C>T
|
XP_011543769.1:p.Gln497Ter
|
|
|
XM_011545468.1:c.1489C>T
|
XP_011543770.1:p.Gln497Ter
|
|
|
XM_011545469.1:c.1489C>T
|
XP_011543771.1:p.Gln497Ter
|
|
|
XM_006724469.3:c.1465C>T
|
XP_006724532.1:p.Gln489Ter
|
|
|
XM_006724470.3:c.1489C>T
|
XP_006724533.1:p.Gln497Ter
|
|
|
XM_006724474.3:c.1489C>T
|
XP_006724537.1:p.Gln497Ter
|
|
|
XM_011545468.2:c.1489C>T
|
XP_011543770.1:p.Gln497Ter
|
|
|
XM_017029328.1:c.1489C>T
|
XP_016884817.1:p.Gln497Ter
|
|
|
XM_017029329.1:c.1489C>T
|
XP_016884818.1:p.Gln497Ter
|
|
|
XM_017029330.2:c.1489C>T
|
XP_016884819.1:p.Gln497Ter
|
|
|
NM_000109.4:c.1465C>T
|
NP_000100.3:p.Gln489Ter
|
|
|
NM_004006.3:c.1489C>T
MANE Select
|
NP_003997.2:p.Gln497Ter
|
|
