ENST00000644900.2:c.2634+2227T>G
|
ENSP00000495641.2:n.2634+2227T>G
|
|
ENST00000233146.7:c.*149T>G
MANE Select
|
ENSP00000233146.2:n.*149T>G
|
|
ENST00000543555.6:c.*149T>G
|
ENSP00000442697.1:n.*149T>G
|
|
ENST00000644092.1:c.*934+2227T>G
|
ENSP00000496351.1:n.*934+2227T>G
|
|
ENST00000644900.1:c.487+2227T>G
|
|
|
ENST00000645339.1:c.2634+2227T>G
|
ENSP00000496441.1:n.2634+2227T>G
|
|
ENST00000645506.1:c.2634+2227T>G
|
ENSP00000495455.1:n.2634+2227T>G
|
|
ENST00000646415.1:c.2634+2227T>G
|
ENSP00000495543.1:n.2634+2227T>G
|
|
ENST00000233146.6:c.*149T>G
|
ENSP00000233146.2:n.*149T>G
|
|
ENST00000406134.5:c.2634+2227T>G
|
ENSP00000384199.1:n.2634+2227T>G
|
|
ENST00000461394.5:n.75+2227T>G
|
|
|
ENST00000543555.5:c.*149T>G
|
ENSP00000442697.1:n.*149T>G
|
|
NM_000251.2:c.*149T>G , LRG_218t1:c.*149T>G
|
NP_000242.1:n.*149T>G
|
|
NM_001258281.1:c.*149T>G
|
NP_001245210.1:n.*149T>G
|
|
XM_005264332.2:c.2634+2227T>G
|
XP_005264389.2:n.2634+2227T>G
|
|
XM_011532867.1:c.2634+2227T>G
|
XP_011531169.1:n.2634+2227T>G
|
|
XR_939685.1:n.2706+2227T>G
|
|
|
XM_005264332.4:c.2634+2227T>G
|
XP_005264389.2:n.2634+2227T>G
|
|
XM_011532867.2:c.2634+2227T>G
|
XP_011531169.1:n.2634+2227T>G
|
|
XR_001738747.2:n.2696+2227T>G
|
|
|
XR_939685.2:n.2696+2227T>G
|
|
|
NM_000251.3:c.*149T>G
MANE Select
|
NP_000242.1:n.*149T>G
|
|