ENST00000645828.1:n.2697C>G
|
|
|
ENST00000651671.1:c.4890C>G
MANE Select
|
ENSP00000498587.1:p.Pro1630=
|
|
ENST00000679595.1:c.4890C>G
|
ENSP00000506241.1:p.Pro1630=
|
|
ENST00000680133.1:c.4776C>G
|
ENSP00000505319.1:p.Pro1592=
|
|
ENST00000680218.1:c.4770C>G
|
ENSP00000505339.1:p.Pro1590=
|
|
ENST00000680668.1:c.4776C>G
|
ENSP00000506336.1:p.Pro1592=
|
|
ENST00000680778.1:c.2487C>G
|
ENSP00000506033.1:p.Pro829=
|
|
ENST00000680924.1:c.*2290C>G
|
ENSP00000506031.1:n.*2290C>G
|
|
ENST00000681135.1:c.*2499C>G
|
ENSP00000506636.1:n.*2499C>G
|
|
ENST00000681298.1:n.1703C>G
|
|
|
ENST00000681454.1:c.*4126C>G
|
ENSP00000505763.1:n.*4126C>G
|
|
ENST00000277541.6:c.4890C>G
|
ENSP00000277541.6:p.Pro1630=
|
|
ENST00000494783.1:n.45C>G
|
|
|
NM_017617.3:c.4890C>G
|
NP_060087.3:p.Pro1630=
|
|
XM_011518717.1:c.4191C>G
|
XP_011517019.1:p.Pro1397=
|
|
NM_017617.5:c.4890C>G
MANE Select
|
NP_060087.3:p.Pro1630=
|
|
XM_011518717.2:c.4167C>G
|
XP_011517019.2:p.Pro1389=
|
|