ENST00000004103.8:c.636G>T
MANE Select
|
ENSP00000004103.3:p.Leu212=
|
|
ENST00000468689.2:c.459G>T
|
ENSP00000420081.2:p.Leu153=
|
|
ENST00000004103.7:c.636G>T
|
ENSP00000004103.3:p.Leu212=
|
|
ENST00000461345.5:c.459G>T
|
ENSP00000420818.1:p.Leu153=
|
|
ENST00000462826.1:n.1778-385G>T
|
|
|
ENST00000474166.1:n.295G>T
|
|
|
ENST00000475007.5:n.532G>T
|
|
|
ENST00000475536.5:c.492G>T
|
ENSP00000417834.1:p.Leu164=
|
|
ENST00000481305.1:n.367-385G>T
|
|
|
ENST00000484928.5:c.636G>T
|
ENSP00000417626.1:p.Leu212=
|
|
ENST00000494349.5:n.1182G>T
|
|
|
NM_018487.2:c.636G>T
|
NP_060957.2:p.Leu212=
|
|
XM_011516376.1:c.687G>T
|
XP_011514678.1:p.Leu229=
|
|
XM_011516377.1:c.687G>T
|
XP_011514679.1:p.Leu229=
|
|
XM_011516378.1:c.607-385G>T
|
XP_011514680.1:n.607-385G>T
|
|
XM_011516376.3:c.687G>T
|
XP_011514678.1:p.Leu229=
|
|
XM_011516377.2:c.687G>T
|
XP_011514679.1:p.Leu229=
|
|
XM_011516378.2:c.607-385G>T
|
XP_011514680.1:n.607-385G>T
|
|
XM_017012393.1:c.636G>T
|
XP_016867882.1:p.Leu212=
|
|
XM_024446824.1:c.556-385G>T
|
XP_024302592.1:n.556-385G>T
|
|
NM_018487.3:c.636G>T
MANE Select
|
NP_060957.2:p.Leu212=
|
|