ENST00000370096.9:c.2655+1G>C
MANE Select
|
ENSP00000359114.3:n.2655+1G>C
|
|
ENST00000353414.8:c.2538+1G>C
|
ENSP00000302551.6:n.2538+1G>C
|
|
ENST00000358392.6:c.2691+1G>C
|
ENSP00000351163.2:n.2691+1G>C
|
|
ENST00000370096.7:c.2655+1G>C
|
ENSP00000359114.3:n.2655+1G>C
|
|
ENST00000512756.5:c.2307+1G>C
|
ENSP00000426533.1:n.2307+1G>C
|
|
ENST00000635193.1:c.1989+1G>C
|
|
|
NM_001190709.1:c.2538+1G>C
|
NP_001177638.1:n.2538+1G>C
|
|
NM_001854.3:c.2655+1G>C
|
NP_001845.3:n.2655+1G>C
|
|
NM_080629.2:c.2691+1G>C
|
NP_542196.2:n.2691+1G>C
|
|
NM_080630.3:c.2307+1G>C
|
NP_542197.3:n.2307+1G>C
|
|
XM_011540719.1:c.2655+1G>C
|
XP_011539021.1:n.2655+1G>C
|
|
XM_011540720.1:c.888+1G>C
|
XP_011539022.1:n.888+1G>C
|
|
XM_011540721.1:c.243+1G>C
|
XP_011539023.1:n.243+1G>C
|
|
XR_946545.1:n.3069+1G>C
|
|
|
NR_134980.1:n.2989+1G>C
|
|
|
XM_017000334.1:c.2808+1G>C
|
XP_016855823.1:n.2808+1G>C
|
|
XM_017000335.1:c.2802+1G>C
|
XP_016855824.1:n.2802+1G>C
|
|
XM_017000336.1:c.2808+1G>C
|
XP_016855825.1:n.2808+1G>C
|
|
XM_017000337.1:c.1206+1G>C
|
XP_016855826.1:n.1206+1G>C
|
|
NM_001854.4:c.2655+1G>C
MANE Select
|
NP_001845.3:n.2655+1G>C
|
|
NM_080630.4:c.2307+1G>C
|
NP_542197.3:n.2307+1G>C
|
|
NR_134980.2:n.3015+1G>C
|
|
|
NM_001190709.2:c.2538+1G>C
|
NP_001177638.1:n.2538+1G>C
|
|
NM_080629.3:c.2691+1G>C
|
NP_542196.2:n.2691+1G>C
|
|