ENST00000340592.10:c.2385+3353C>T
|
ENSP00000339343.5:n.2385+3353C>T
|
|
ENST00000706733.1:c.2508+3353C>T
|
ENSP00000516520.1:n.2508+3353C>T
|
|
ENST00000706734.1:c.2412+3353C>T
|
ENSP00000516521.1:n.2412+3353C>T
|
|
ENST00000285900.10:c.2386-3413C>T
MANE Select
|
ENSP00000285900.4:n.2386-3413C>T
|
|
ENST00000285900.9:c.2386-3413C>T
|
ENSP00000285900.4:n.2386-3413C>T
|
|
ENST00000340592.9:c.2385+3353C>T
|
ENSP00000339343.5:n.2385+3353C>T
|
|
ENST00000448073.8:c.2415+3353C>T
|
ENSP00000415569.2:n.2415+3353C>T
|
|
ENST00000518142.5:c.2146-3413C>T
|
ENSP00000427920.1:n.2146-3413C>T
|
|
ENST00000518783.1:c.2416-3413C>T
|
ENSP00000428994.1:n.2416-3413C>T
|
|
ENST00000521843.6:c.2179-3413C>T
|
ENSP00000427864.2:n.2179-3413C>T
|
|
NM_000827.3:c.2386-3413C>T
|
NP_000818.2:n.2386-3413C>T
|
|
NM_001114183.1:c.2385+3353C>T
|
NP_001107655.1:n.2385+3353C>T
|
|
NM_001258019.1:c.2146-3413C>T
|
NP_001244948.1:n.2146-3413C>T
|
|
NM_001258020.1:c.2100+3353C>T
|
NP_001244949.1:n.2100+3353C>T
|
|
NM_001258021.1:c.2416-3413C>T
|
NP_001244950.1:n.2416-3413C>T
|
|
NM_001258022.1:c.2415+3353C>T
|
NP_001244951.1:n.2415+3353C>T
|
|
NM_001258023.1:c.2179-3413C>T
|
NP_001244952.1:n.2179-3413C>T
|
|
NR_047578.1:n.2498-3413C>T
|
|
|
XM_011537635.1:c.2325+3353C>T
|
XP_011535937.1:n.2325+3353C>T
|
|
XR_427776.2:n.2541-3413C>T
|
|
|
NM_001364165.1:c.2218-3413C>T
|
NP_001351094.1:n.2218-3413C>T
|
|
NM_001364166.1:c.2412+3353C>T
|
NP_001351095.1:n.2412+3353C>T
|
|
NM_001364167.1:c.2178+3353C>T
|
NP_001351096.1:n.2178+3353C>T
|
|
NR_157093.1:n.2719+3353C>T
|
|
|
XM_017009392.1:c.2426-3413C>T
|
XP_016864881.1:n.2426-3413C>T
|
|
NM_000827.4:c.2386-3413C>T
MANE Select
|
NP_000818.2:n.2386-3413C>T
|
|
NM_001114183.2:c.2385+3353C>T
|
NP_001107655.1:n.2385+3353C>T
|
|
NM_001258019.2:c.2146-3413C>T
|
NP_001244948.1:n.2146-3413C>T
|
|
NM_001258020.2:c.2100+3353C>T
|
NP_001244949.1:n.2100+3353C>T
|
|
NM_001258021.2:c.2416-3413C>T
|
NP_001244950.1:n.2416-3413C>T
|
|
NM_001258022.2:c.2415+3353C>T
|
NP_001244951.1:n.2415+3353C>T
|
|
NM_001364165.2:c.2218-3413C>T
|
NP_001351094.1:n.2218-3413C>T
|
|
NM_001364166.2:c.2412+3353C>T
|
NP_001351095.1:n.2412+3353C>T
|
|
NM_001364167.2:c.2178+3353C>T
|
NP_001351096.1:n.2178+3353C>T
|
|
NR_047578.2:n.2352-3413C>T
|
|
|
NR_157093.2:n.2719+3353C>T
|
|
|