ENST00000645828.1:n.2587C>G
|
|
|
ENST00000651671.1:c.4780C>G
MANE Select
|
ENSP00000498587.1:p.Arg1594Gly
|
|
ENST00000679595.1:c.4780C>G
|
ENSP00000506241.1:p.Arg1594Gly
|
|
ENST00000680133.1:c.4666C>G
|
ENSP00000505319.1:p.Arg1556Gly
|
|
ENST00000680218.1:c.4660C>G
|
ENSP00000505339.1:p.Arg1554Gly
|
|
ENST00000680668.1:c.4666C>G
|
ENSP00000506336.1:p.Arg1556Gly
|
|
ENST00000680778.1:c.2377C>G
|
ENSP00000506033.1:p.Arg793Gly
|
|
ENST00000680924.1:c.*2180C>G
|
ENSP00000506031.1:n.*2180C>G
|
|
ENST00000681135.1:c.*2389C>G
|
ENSP00000506636.1:n.*2389C>G
|
|
ENST00000681298.1:n.1593C>G
|
|
|
ENST00000681454.1:c.*4016C>G
|
ENSP00000505763.1:n.*4016C>G
|
|
ENST00000277541.6:c.4780C>G
|
ENSP00000277541.6:p.Arg1594Gly
|
|
NM_017617.3:c.4780C>G
|
NP_060087.3:p.Arg1594Gly
|
|
XM_011518717.1:c.4081C>G
|
XP_011517019.1:p.Arg1361Gly
|
|
NM_017617.5:c.4780C>G
MANE Select
|
NP_060087.3:p.Arg1594Gly
|
|
XM_011518717.2:c.4057C>G
|
XP_011517019.2:p.Arg1353Gly
|
|