ENST00000004103.8:c.618T>G
MANE Select
|
ENSP00000004103.3:p.Ser206=
|
|
ENST00000468689.2:c.441T>G
|
ENSP00000420081.2:p.Ser147=
|
|
ENST00000004103.7:c.618T>G
|
ENSP00000004103.3:p.Ser206=
|
|
ENST00000461345.5:c.441T>G
|
ENSP00000420818.1:p.Ser147=
|
|
ENST00000462826.1:n.1778-403T>G
|
|
|
ENST00000474166.1:n.277T>G
|
|
|
ENST00000475007.5:n.514T>G
|
|
|
ENST00000475536.5:c.474T>G
|
ENSP00000417834.1:p.Ser158=
|
|
ENST00000481305.1:n.367-403T>G
|
|
|
ENST00000484928.5:c.618T>G
|
ENSP00000417626.1:p.Ser206=
|
|
ENST00000494349.5:n.1164T>G
|
|
|
NM_018487.2:c.618T>G
|
NP_060957.2:p.Ser206=
|
|
XM_011516376.1:c.669T>G
|
XP_011514678.1:p.Ser223=
|
|
XM_011516377.1:c.669T>G
|
XP_011514679.1:p.Ser223=
|
|
XM_011516378.1:c.607-403T>G
|
XP_011514680.1:n.607-403T>G
|
|
XM_011516376.3:c.669T>G
|
XP_011514678.1:p.Ser223=
|
|
XM_011516377.2:c.669T>G
|
XP_011514679.1:p.Ser223=
|
|
XM_011516378.2:c.607-403T>G
|
XP_011514680.1:n.607-403T>G
|
|
XM_017012393.1:c.618T>G
|
XP_016867882.1:p.Ser206=
|
|
XM_024446824.1:c.556-403T>G
|
XP_024302592.1:n.556-403T>G
|
|
NM_018487.3:c.618T>G
MANE Select
|
NP_060957.2:p.Ser206=
|
|