ENST00000391944.8:c.2047-6C>T
|
ENSP00000375808.4:n.2047-6C>T
|
|
ENST00000682414.1:c.2047-6C>T
|
ENSP00000507019.1:n.2047-6C>T
|
|
ENST00000682508.1:n.2076-6C>T
|
|
|
ENST00000684218.1:c.*1305-6C>T
|
ENSP00000507804.1:n.*1305-6C>T
|
|
ENST00000684264.1:n.1603-6C>T
|
|
|
ENST00000684407.1:c.1924-6C>T
|
ENSP00000507775.1:n.1924-6C>T
|
|
ENST00000684458.1:c.*533-6C>T
|
ENSP00000508260.1:n.*533-6C>T
|
|
ENST00000684468.1:n.1759-6C>T
|
|
|
ENST00000391945.10:c.2047-6C>T
MANE Select
|
ENSP00000375809.4:n.2047-6C>T
|
|
ENST00000646507.1:n.2144-6C>T
|
|
|
ENST00000391941.6:c.1975-6C>T
|
ENSP00000375805.2:n.1975-6C>T
|
|
ENST00000391942.6:n.1218-6C>T
|
|
|
ENST00000391944.7:c.1813-6C>T
|
ENSP00000375808.3:n.1813-6C>T
|
|
ENST00000391945.8:c.2047-6C>T
|
ENSP00000375809.3:n.2047-6C>T
|
|
ENST00000588652.5:n.2135-6C>T
|
|
|
NM_000400.3:c.2047-6C>T , LRG_461t1:c.2047-6C>T
|
NP_000391.1:n.2047-6C>T
|
|
XM_011526611.1:c.1969-6C>T
|
XP_011524913.1:n.1969-6C>T
|
|
XM_011526611.2:c.1969-6C>T
|
XP_011524913.1:n.1969-6C>T
|
|
XM_017026467.1:c.1924-6C>T
|
XP_016881956.1:n.1924-6C>T
|
|
XR_001753633.2:n.2094-6C>T
|
|
|
XR_001753634.2:n.2030-6C>T
|
|
|
NM_000400.4:c.2047-6C>T
MANE Select
|
NP_000391.1:n.2047-6C>T
|
|