ENST00000526189.3:c.367+136G>C
|
ENSP00000488104.2:n.367+136G>C
|
|
ENST00000533357.5:c.448+55G>C
MANE Select
|
ENSP00000432943.1:n.448+55G>C
|
|
ENST00000672287.2:c.-141+55G>C
|
ENSP00000499818.2:n.-141+55G>C
|
|
ENST00000672602.2:c.448+55G>C
|
ENSP00000500814.2:n.448+55G>C
|
|
ENST00000674861.1:n.511+55G>C
|
|
|
ENST00000463290.5:c.448+55G>C
|
ENSP00000431538.1:n.448+55G>C
|
|
ENST00000491222.5:c.-141+55G>C
|
ENSP00000431441.1:n.-141+55G>C
|
|
ENST00000526189.2:c.111+136G>C
|
|
|
ENST00000533357.4:c.448+55G>C
|
ENSP00000432943.1:n.448+55G>C
|
|
NM_000530.6:c.448+55G>C , LRG_256t1:c.448+55G>C
|
NP_000521.2:n.448+55G>C
|
|
NM_000530.7:c.448+55G>C
|
NP_000521.2:n.448+55G>C
|
|
NM_001315491.1:c.448+55G>C
|
NP_001302420.1:n.448+55G>C
|
|
XM_017001321.2:c.478+55G>C
|
XP_016856810.1:n.478+55G>C
|
|
NM_000530.8:c.448+55G>C
MANE Select
|
NP_000521.2:n.448+55G>C
|
|
NM_001315491.2:c.448+55G>C
|
NP_001302420.1:n.448+55G>C
|
|