ENST00000333681.5:c.*784G>C
MANE Select
|
ENSP00000329623.3:n.*784G>C
|
|
ENST00000677227.1:c.1832G>C
|
ENSP00000504566.1:n.1832G>C
|
|
ENST00000677635.1:n.1068G>C
|
|
|
ENST00000678134.1:c.1708G>C
|
ENSP00000503628.1:n.1708G>C
|
|
ENST00000678301.1:c.*784G>C
|
ENSP00000504546.1:n.*784G>C
|
|
ENST00000678349.1:c.2056G>C
|
ENSP00000504190.1:n.2056G>C
|
|
ENST00000333681.4:c.*784G>C
|
ENSP00000329623.3:n.*784G>C
|
|
ENST00000398117.1:c.*784G>C
|
ENSP00000381185.1:n.*784G>C
|
|
NM_000633.2:c.*784G>C
|
NP_000624.2:n.*784G>C
|
|
NM_000633.3:c.*784G>C
MANE Select
|
NP_000624.2:n.*784G>C
|
|