ENST00000324041.6:c.612+126G>C
MANE Select
|
ENSP00000326159.1:n.612+126G>C
|
|
ENST00000324041.5:c.612+126G>C
|
ENSP00000326159.1:n.612+126G>C
|
|
ENST00000431178.2:c.328+346G>C
|
ENSP00000399448.2:n.328+346G>C
|
|
ENST00000593885.1:c.*107+126G>C
|
ENSP00000469769.1:n.*107+126G>C
|
|
ENST00000596876.1:n.740G>C
|
|
|
ENST00000598305.5:c.*107+126G>C
|
ENSP00000469963.1:n.*107+126G>C
|
|
ENST00000599865.5:n.548+126G>C
|
|
|
ENST00000602148.1:c.624+126G>C
|
ENSP00000472091.1:n.624+126G>C
|
|
NM_001302961.1:c.327+126G>C
|
NP_001289890.1:n.327+126G>C
|
|
NM_004917.4:c.612+126G>C
|
NP_004908.4:n.612+126G>C
|
|
NR_126566.1:n.601+126G>C
|
|
|
XM_005259441.3:c.327+126G>C
|
XP_005259498.2:n.327+126G>C
|
|
XM_011527546.1:c.475+346G>C
|
XP_011525848.1:n.475+346G>C
|
|
XM_011527547.1:c.465+126G>C
|
XP_011525849.1:n.465+126G>C
|
|
XM_005259441.4:c.327+126G>C
|
XP_005259498.2:n.327+126G>C
|
|
XM_011527546.2:c.475+346G>C
|
XP_011525848.1:n.475+346G>C
|
|
NM_001302961.2:c.327+126G>C
|
NP_001289890.1:n.327+126G>C
|
|
NR_126566.2:n.601+126G>C
|
|
|
NM_004917.5:c.612+126G>C
MANE Select
|
NP_004908.4:n.612+126G>C
|
|