ENST00000324041.6:c.612+245T>C
MANE Select
|
ENSP00000326159.1:n.612+245T>C
|
|
ENST00000324041.5:c.612+245T>C
|
ENSP00000326159.1:n.612+245T>C
|
|
ENST00000431178.2:c.328+465T>C
|
ENSP00000399448.2:n.328+465T>C
|
|
ENST00000593885.1:c.*107+245T>C
|
ENSP00000469769.1:n.*107+245T>C
|
|
ENST00000596876.1:n.859T>C
|
|
|
ENST00000598305.5:c.*107+245T>C
|
ENSP00000469963.1:n.*107+245T>C
|
|
ENST00000599865.5:n.548+245T>C
|
|
|
ENST00000602148.1:c.624+245T>C
|
ENSP00000472091.1:n.624+245T>C
|
|
NM_001302961.1:c.327+245T>C
|
NP_001289890.1:n.327+245T>C
|
|
NM_004917.4:c.612+245T>C
|
NP_004908.4:n.612+245T>C
|
|
NR_126566.1:n.601+245T>C
|
|
|
XM_005259441.3:c.327+245T>C
|
XP_005259498.2:n.327+245T>C
|
|
XM_011527546.1:c.475+465T>C
|
XP_011525848.1:n.475+465T>C
|
|
XM_011527547.1:c.465+245T>C
|
XP_011525849.1:n.465+245T>C
|
|
XM_005259441.4:c.327+245T>C
|
XP_005259498.2:n.327+245T>C
|
|
XM_011527546.2:c.475+465T>C
|
XP_011525848.1:n.475+465T>C
|
|
NM_001302961.2:c.327+245T>C
|
NP_001289890.1:n.327+245T>C
|
|
NR_126566.2:n.601+245T>C
|
|
|
NM_004917.5:c.612+245T>C
MANE Select
|
NP_004908.4:n.612+245T>C
|
|