ENST00000372563.2:c.1045-22A>G
MANE Select
|
ENSP00000361644.1:n.1045-22A>G
|
|
ENST00000327674.8:c.1045-22A>G
|
ENSP00000329374.4:n.1045-22A>G
|
|
ENST00000372563.1:c.1045-22A>G
|
ENSP00000361644.1:n.1045-22A>G
|
|
ENST00000487487.1:n.357A>G
|
|
|
NM_000354.5:c.1045-22A>G
|
NP_000345.2:n.1045-22A>G
|
|
XM_005262180.3:c.1084A>G
|
XP_005262237.1:p.Arg362Gly
|
|
XM_006724683.1:c.1053A>G
|
XP_006724746.1:p.Ala351=
|
|
XM_005262180.4:c.1084A>G
|
XP_005262237.1:p.Arg362Gly
|
|
XM_006724683.2:c.1053A>G
|
XP_006724746.1:p.Ala351=
|
|
NM_000354.6:c.1045-22A>G
MANE Select
|
NP_000345.2:n.1045-22A>G
|
|