ENST00000004103.8:c.617C>A
MANE Select
|
ENSP00000004103.3:p.Ser206Tyr
|
|
ENST00000468689.2:c.440C>A
|
ENSP00000420081.2:p.Ser147Tyr
|
|
ENST00000004103.7:c.617C>A
|
ENSP00000004103.3:p.Ser206Tyr
|
|
ENST00000461345.5:c.440C>A
|
ENSP00000420818.1:p.Ser147Tyr
|
|
ENST00000462826.1:n.1778-404C>A
|
|
|
ENST00000474166.1:n.276C>A
|
|
|
ENST00000475007.5:n.513C>A
|
|
|
ENST00000475536.5:c.473C>A
|
ENSP00000417834.1:p.Ser158Tyr
|
|
ENST00000481305.1:n.367-404C>A
|
|
|
ENST00000484928.5:c.617C>A
|
ENSP00000417626.1:p.Ser206Tyr
|
|
ENST00000494349.5:n.1163C>A
|
|
|
NM_018487.2:c.617C>A
|
NP_060957.2:p.Ser206Tyr
|
|
XM_011516376.1:c.668C>A
|
XP_011514678.1:p.Ser223Tyr
|
|
XM_011516377.1:c.668C>A
|
XP_011514679.1:p.Ser223Tyr
|
|
XM_011516378.1:c.607-404C>A
|
XP_011514680.1:n.607-404C>A
|
|
XM_011516376.3:c.668C>A
|
XP_011514678.1:p.Ser223Tyr
|
|
XM_011516377.2:c.668C>A
|
XP_011514679.1:p.Ser223Tyr
|
|
XM_011516378.2:c.607-404C>A
|
XP_011514680.1:n.607-404C>A
|
|
XM_017012393.1:c.617C>A
|
XP_016867882.1:p.Ser206Tyr
|
|
XM_024446824.1:c.556-404C>A
|
XP_024302592.1:n.556-404C>A
|
|
NM_018487.3:c.617C>A
MANE Select
|
NP_060957.2:p.Ser206Tyr
|
|