ENST00000249806.11:c.*562G>T
MANE Select
|
ENSP00000249806.5:n.*562G>T
|
|
ENST00000562767.2:c.84-9950G>T
|
ENSP00000456336.1:n.84-9950G>T
|
|
ENST00000636964.1:n.3026G>T
|
|
|
ENST00000637054.1:c.199-9950G>T
|
ENSP00000490807.1:n.199-9950G>T
|
|
ENST00000637888.1:c.199-9950G>T
|
ENSP00000490546.1:n.199-9950G>T
|
|
ENST00000638026.1:n.103G>T
|
|
|
ENST00000638076.1:c.*1101G>T
|
ENSP00000490373.1:n.*1101G>T
|
|
ENST00000646164.1:c.39-7897G>T
|
|
|
ENST00000249806.9:c.*562G>T
|
ENSP00000249806.5:n.*562G>T
|
|
ENST00000562767.1:c.84-9950G>T
|
ENSP00000456336.1:n.84-9950G>T
|
|
NM_017882.2:c.*562G>T
|
NP_060352.1:n.*562G>T
|
|
NM_017882.3:c.*562G>T
MANE Select
|
NP_060352.1:n.*562G>T
|
|