ENST00000004103.8:c.556-94G>C
MANE Select
|
ENSP00000004103.3:n.556-94G>C
|
|
ENST00000468689.2:c.379-94G>C
|
ENSP00000420081.2:n.379-94G>C
|
|
ENST00000004103.7:c.556-94G>C
|
ENSP00000004103.3:n.556-94G>C
|
|
ENST00000461345.5:c.379-94G>C
|
ENSP00000420818.1:n.379-94G>C
|
|
ENST00000462826.1:n.1777+436G>C
|
|
|
ENST00000474166.1:n.215-94G>C
|
|
|
ENST00000475007.5:n.452-94G>C
|
|
|
ENST00000475536.5:c.412-94G>C
|
ENSP00000417834.1:n.412-94G>C
|
|
ENST00000481305.1:n.366+436G>C
|
|
|
ENST00000484928.5:c.556-94G>C
|
ENSP00000417626.1:n.556-94G>C
|
|
ENST00000494349.5:n.1102-94G>C
|
|
|
NM_018487.2:c.556-94G>C
|
NP_060957.2:n.556-94G>C
|
|
XM_011516376.1:c.607-94G>C
|
XP_011514678.1:n.607-94G>C
|
|
XM_011516377.1:c.607-94G>C
|
XP_011514679.1:n.607-94G>C
|
|
XM_011516378.1:c.606+436G>C
|
XP_011514680.1:n.606+436G>C
|
|
XM_011516376.3:c.607-94G>C
|
XP_011514678.1:n.607-94G>C
|
|
XM_011516377.2:c.607-94G>C
|
XP_011514679.1:n.607-94G>C
|
|
XM_011516378.2:c.606+436G>C
|
XP_011514680.1:n.606+436G>C
|
|
XM_017012393.1:c.556-94G>C
|
XP_016867882.1:n.556-94G>C
|
|
XM_024446824.1:c.555+436G>C
|
XP_024302592.1:n.555+436G>C
|
|
NM_018487.3:c.556-94G>C
MANE Select
|
NP_060957.2:n.556-94G>C
|
|