ENST00000585361.6:c.*623C>G
|
ENSP00000466983.1:n.*623C>G
|
|
ENST00000588558.6:c.*761C>G
|
ENSP00000467624.1:n.*761C>G
|
|
ENST00000590253.3:c.*79C>G
|
ENSP00000465111.2:n.*79C>G
|
|
ENST00000593115.2:c.*807C>G
|
ENSP00000466821.1:n.*807C>G
|
|
ENST00000696383.1:c.441C>G
|
ENSP00000512593.1:p.Gly147=
|
|
ENST00000696384.1:c.*346C>G
|
ENSP00000512594.1:n.*346C>G
|
|
ENST00000696385.1:c.*504C>G
|
ENSP00000512595.1:n.*504C>G
|
|
ENST00000696386.1:c.*79C>G
|
ENSP00000512596.1:n.*79C>G
|
|
ENST00000696387.1:c.*413C>G
|
ENSP00000512597.1:n.*413C>G
|
|
ENST00000696388.1:c.*632C>G
|
ENSP00000512598.1:n.*632C>G
|
|
ENST00000696389.1:c.*817C>G
|
ENSP00000512599.1:n.*817C>G
|
|
ENST00000696390.1:c.576C>G
|
ENSP00000512600.1:p.Gly192=
|
|
ENST00000696391.1:c.*642C>G
|
ENSP00000512601.1:n.*642C>G
|
|
ENST00000696392.1:c.786C>G
|
ENSP00000512602.1:p.Gly262=
|
|
ENST00000696393.1:c.786C>G
|
ENSP00000512603.1:p.Gly262=
|
|
ENST00000696405.1:c.677+337C>G
|
ENSP00000512607.1:n.677+337C>G
|
|
ENST00000269097.9:c.786C>G
MANE Select
|
ENSP00000269097.3:p.Gly262=
|
|
ENST00000269097.8:c.786C>G
|
ENSP00000269097.3:p.Gly262=
|
|
ENST00000585361.5:c.*623C>G
|
ENSP00000466983.1:n.*623C>G
|
|
ENST00000588558.5:c.*761C>G
|
ENSP00000467624.1:n.*761C>G
|
|
ENST00000590253.2:c.288C>G
|
|
|
ENST00000590639.1:n.807C>G
|
|
|
ENST00000591696.1:c.678C>G
|
ENSP00000468677.1:p.Gly226=
|
|
NM_138387.3:c.786C>G , LRG_182t1:c.786C>G
|
NP_612396.1:p.Gly262=
|
|
NR_028581.1:n.1216C>G
|
|
|
NR_028582.1:n.1081C>G
|
|
|
XM_011525473.1:c.441C>G
|
XP_011523775.1:p.Gly147=
|
|
XM_011525474.1:c.441C>G
|
XP_011523776.1:p.Gly147=
|
|
NM_001319945.1:c.*79C>G
|
NP_001306874.1:n.*79C>G
|
|
XM_011525473.3:c.441C>G
|
XP_011523775.1:p.Gly147=
|
|
XM_011525474.3:c.441C>G
|
XP_011523776.1:p.Gly147=
|
|
XM_017025335.2:c.441C>G
|
XP_016880824.1:p.Gly147=
|
|
NM_001319945.2:c.*79C>G
|
NP_001306874.1:n.*79C>G
|
|
NR_028581.2:n.1035C>G
|
|
|
NR_028582.2:n.900C>G
|
|
|
NM_001384165.1:c.441C>G
|
NP_001371094.1:p.Gly147=
|
|
NM_001384166.1:c.441C>G
|
NP_001371095.1:p.Gly147=
|
|
NM_001384167.1:c.441C>G
|
NP_001371096.1:p.Gly147=
|
|
NM_001384168.1:c.441C>G
|
NP_001371097.1:p.Gly147=
|
|
NM_138387.4:c.786C>G
MANE Select
|
NP_612396.1:p.Gly262=
|
|