ENST00000374479.4:c.1155T>G
MANE Select
|
ENSP00000363603.3:p.Ser385=
|
|
ENST00000374479.3:c.1155T>G
|
ENSP00000363603.3:p.Ser385=
|
|
NM_000147.4:c.1155T>G
|
NP_000138.2:p.Ser385=
|
|
XM_005245821.1:c.780T>G
|
XP_005245878.1:p.Ser260=
|
|
XM_011541167.1:c.522T>G
|
XP_011539469.1:p.Ser174=
|
|
XM_005245821.3:c.780T>G
|
XP_005245878.1:p.Ser260=
|
|
XM_011541167.3:c.522T>G
|
XP_011539469.1:p.Ser174=
|
|
XM_017000905.2:c.852T>G
|
XP_016856394.1:p.Ser284=
|
|
NM_000147.5:c.1155T>G
MANE Select
|
NP_000138.2:p.Ser385=
|
|
NR_174379.1:n.1333T>G
|
|
|
NR_174380.1:n.1382T>G
|
|
|
NR_174381.1:n.1221T>G
|
|
|
NR_174382.1:n.1618T>G
|
|
|