ENST00000645828.1:n.2716G>C
|
|
|
ENST00000651671.1:c.4909G>C
MANE Select
|
ENSP00000498587.1:p.Gly1637Arg
|
|
ENST00000679595.1:c.4909G>C
|
ENSP00000506241.1:p.Gly1637Arg
|
|
ENST00000680133.1:c.4795G>C
|
ENSP00000505319.1:p.Gly1599Arg
|
|
ENST00000680218.1:c.4789G>C
|
ENSP00000505339.1:p.Gly1597Arg
|
|
ENST00000680668.1:c.4795G>C
|
ENSP00000506336.1:p.Gly1599Arg
|
|
ENST00000680778.1:c.2506G>C
|
ENSP00000506033.1:p.Gly836Arg
|
|
ENST00000680924.1:c.*2309G>C
|
ENSP00000506031.1:n.*2309G>C
|
|
ENST00000681135.1:c.*2518G>C
|
ENSP00000506636.1:n.*2518G>C
|
|
ENST00000681298.1:n.1722G>C
|
|
|
ENST00000681454.1:c.*4145G>C
|
ENSP00000505763.1:n.*4145G>C
|
|
ENST00000277541.6:c.4909G>C
|
ENSP00000277541.6:p.Gly1637Arg
|
|
ENST00000494783.1:n.64G>C
|
|
|
NM_017617.3:c.4909G>C
|
NP_060087.3:p.Gly1637Arg
|
|
XM_011518717.1:c.4210G>C
|
XP_011517019.1:p.Gly1404Arg
|
|
NM_017617.5:c.4909G>C
MANE Select
|
NP_060087.3:p.Gly1637Arg
|
|
XM_011518717.2:c.4186G>C
|
XP_011517019.2:p.Gly1396Arg
|
|