ENST00000534010.2:c.314+6324G>T
|
ENSP00000433202.2:n.314+6324G>T
|
|
ENST00000375549.8:c.*365G>T
MANE Select
|
ENSP00000364699.3:n.*365G>T
|
|
ENST00000528021.6:c.314+6324G>T
|
ENSP00000432465.1:n.314+6324G>T
|
|
ENST00000375549.7:c.*365G>T
|
ENSP00000364699.3:n.*365G>T
|
|
ENST00000525291.5:c.*365G>T
|
ENSP00000436669.1:n.*365G>T
|
|
ENST00000525987.5:n.319+6324G>T
|
|
|
ENST00000528021.5:c.314+6324G>T
|
ENSP00000432465.1:n.314+6324G>T
|
|
ENST00000528048.5:c.*442G>T
|
ENSP00000436217.1:n.*442G>T
|
|
ENST00000531744.5:c.314+6324G>T
|
ENSP00000456957.1:n.314+6324G>T
|
|
ENST00000532699.1:c.314+6324G>T
|
ENSP00000456434.1:n.314+6324G>T
|
|
ENST00000534010.1:c.145+6324G>T
|
|
|
NM_001276503.1:c.*442G>T
|
NP_001263432.1:n.*442G>T
|
|
NM_001276504.1:c.*365G>T
|
NP_001263433.1:n.*365G>T
|
|
NM_001276506.1:c.*543G>T
|
NP_001263435.1:n.*543G>T
|
|
NM_003002.3:c.*365G>T
|
NP_002993.1:n.*365G>T
|
|
NR_077060.1:n.983G>T
|
|
|
NM_003002.4:c.*365G>T
MANE Select
|
NP_002993.1:n.*365G>T
|
|
NM_001276503.2:c.*442G>T
|
NP_001263432.1:n.*442G>T
|
|
NM_001276504.2:c.*365G>T
|
NP_001263433.1:n.*365G>T
|
|
NM_001276506.2:c.*543G>T
|
NP_001263435.1:n.*543G>T
|
|
NR_077060.2:n.934G>T
|
|
|