ENST00000257895.10:c.569+14G>T
MANE Select
|
ENSP00000257895.6:n.569+14G>T
|
|
ENST00000257895.9:c.569+14G>T
|
ENSP00000257895.5:n.569+14G>T
|
|
ENST00000257899.3:c.591+7G>T
|
|
|
ENST00000547072.5:c.278+14G>T
|
ENSP00000449927.1:n.278+14G>T
|
|
ENST00000548082.1:c.569+14G>T
|
ENSP00000447128.1:n.569+14G>T
|
|
ENST00000548123.1:c.300+467G>T
|
|
|
ENST00000548486.1:n.593G>T
|
|
|
ENST00000550412.5:c.*255G>T
|
ENSP00000447650.1:n.*255G>T
|
|
ENST00000550608.1:n.722G>T
|
|
|
ENST00000551946.5:c.*386G>T
|
ENSP00000450201.1:n.*386G>T
|
|
ENST00000553160.1:n.406-234G>T
|
|
|
ENST00000553187.5:n.593G>T
|
|
|
NM_001199771.1:c.569+14G>T
|
NP_001186700.1:n.569+14G>T
|
|
NM_002905.3:c.569+14G>T
|
NP_002896.2:n.569+14G>T
|
|
NR_037658.1:n.628+14G>T
|
|
|
NM_001199771.2:c.569+14G>T
|
NP_001186700.1:n.569+14G>T
|
|
NM_002905.5:c.569+14G>T
MANE Select
|
NP_002896.2:n.569+14G>T
|
|
NM_001199771.3:c.569+14G>T
|
NP_001186700.1:n.569+14G>T
|
|