ENST00000651671.1:c.6412C>G
MANE Select
|
ENSP00000498587.1:p.Pro2138Ala
|
|
ENST00000679595.1:c.*1452C>G
|
ENSP00000506241.1:n.*1452C>G
|
|
ENST00000679969.1:n.3008C>G
|
|
|
ENST00000680003.1:n.2744C>G
|
|
|
ENST00000680133.1:c.6298C>G
|
ENSP00000505319.1:p.Pro2100Ala
|
|
ENST00000680218.1:c.6292C>G
|
ENSP00000505339.1:p.Pro2098Ala
|
|
ENST00000680668.1:c.6298C>G
|
ENSP00000506336.1:p.Pro2100Ala
|
|
ENST00000680778.1:c.4009C>G
|
ENSP00000506033.1:p.Pro1337Ala
|
|
ENST00000680924.1:c.*3812C>G
|
ENSP00000506031.1:n.*3812C>G
|
|
ENST00000681135.1:c.*4021C>G
|
ENSP00000506636.1:n.*4021C>G
|
|
ENST00000681298.1:n.4517C>G
|
|
|
ENST00000681454.1:c.*5648C>G
|
ENSP00000505763.1:n.*5648C>G
|
|
ENST00000277541.6:c.6412C>G
|
ENSP00000277541.6:p.Pro2138Ala
|
|
NM_017617.3:c.6412C>G
|
NP_060087.3:p.Pro2138Ala
|
|
XM_011518717.1:c.5713C>G
|
XP_011517019.1:p.Pro1905Ala
|
|
NM_017617.5:c.6412C>G
MANE Select
|
NP_060087.3:p.Pro2138Ala
|
|
XM_011518717.2:c.5689C>G
|
XP_011517019.2:p.Pro1897Ala
|
|