ENST00000230538.12:c.2353+131A>G
MANE Select
|
ENSP00000230538.7:n.2353+131A>G
|
|
ENST00000389463.9:c.2332+131A>G
|
ENSP00000374114.4:n.2332+131A>G
|
|
ENST00000651860.1:c.223+131A>G
|
ENSP00000498842.1:n.223+131A>G
|
|
ENST00000230538.11:c.2353+131A>G
|
ENSP00000230538.7:n.2353+131A>G
|
|
ENST00000389463.8:c.2332+131A>G
|
ENSP00000374114.4:n.2332+131A>G
|
|
ENST00000424408.6:c.2332+131A>G
|
ENSP00000416470.2:n.2332+131A>G
|
|
ENST00000522006.5:c.2332+131A>G
|
ENSP00000429488.1:n.2332+131A>G
|
|
ENST00000523765.1:c.765+131A>G
|
|
|
NM_001105206.2:c.2353+131A>G
|
NP_001098676.2:n.2353+131A>G
|
|
NM_001105207.2:c.2332+131A>G
|
NP_001098677.2:n.2332+131A>G
|
|
NM_002290.4:c.2332+131A>G
|
NP_002281.3:n.2332+131A>G
|
|
XM_005266983.3:c.2353+131A>G
|
XP_005267040.2:n.2353+131A>G
|
|
XM_005266984.3:c.2353+131A>G
|
XP_005267041.2:n.2353+131A>G
|
|
XM_011535821.1:c.2353+131A>G
|
XP_011534123.1:n.2353+131A>G
|
|
XM_005266983.4:c.2353+131A>G
|
XP_005267040.2:n.2353+131A>G
|
|
XM_005266984.4:c.2353+131A>G
|
XP_005267041.2:n.2353+131A>G
|
|
XM_017010854.2:c.2332+131A>G
|
XP_016866343.1:n.2332+131A>G
|
|
XR_001743406.2:n.2624+131A>G
|
|
|
XR_001743407.2:n.2603+131A>G
|
|
|
XR_001744299.1:n.429-7294T>C
|
|
|
NM_001105206.3:c.2353+131A>G
MANE Select
|
NP_001098676.2:n.2353+131A>G
|
|
NM_001105207.3:c.2332+131A>G
|
NP_001098677.2:n.2332+131A>G
|
|
NM_002290.5:c.2332+131A>G
|
NP_002281.3:n.2332+131A>G
|
|