ENST00000512905.6:c.23C>G
|
|
|
ENST00000647941.2:c.1137C>G
MANE Select
|
ENSP00000497326.1:p.Pro379=
|
|
ENST00000264193.2:c.1137C>G
|
ENSP00000264193.2:p.Pro379=
|
|
ENST00000510489.1:n.387C>G
|
|
|
ENST00000512905.5:c.23C>G
|
|
|
NM_000097.5:c.1137C>G
|
NP_000088.3:p.Pro379=
|
|
XM_005247125.3:c.1137C>G
|
XP_005247182.1:p.Pro379=
|
|
NM_000097.7:c.1137C>G
MANE Select
|
NP_000088.3:p.Pro379=
|
|
XM_005247125.4:c.1137C>G
|
XP_005247182.1:p.Pro379=
|
|
XR_001740025.2:n.1308C>G
|
|
|
XR_001740026.1:n.1872C>G
|
|
|
XR_001740027.1:n.1412C>G
|
|
|
XR_001740028.1:n.1378C>G
|
|
|