ENST00000509700.2:c.671+386G>T
|
|
|
ENST00000636689.1:n.95-2100G>T
|
|
|
ENST00000637644.1:c.487+598G>T
|
ENSP00000490282.1:n.487+598G>T
|
|
ENST00000638728.1:c.1085G>T
|
ENSP00000492619.1:p.Arg362Met
|
|
ENST00000638840.1:c.807G>T
|
|
|
ENST00000638868.1:c.1085G>T
|
ENSP00000491250.1:p.Arg362Met
|
|
ENST00000639408.1:c.487+598G>T
|
ENSP00000491635.1:n.487+598G>T
|
|
ENST00000640017.1:c.669+386G>T
|
ENSP00000491337.1:n.669+386G>T
|
|
ENST00000640914.1:c.124+386G>T
|
|
|
ENST00000644903.1:c.1085G>T
MANE Select
|
ENSP00000495557.1:p.Arg362Met
|
|
ENST00000368089.3:c.1085G>T
|
ENSP00000357068.3:p.Arg362Met
|
|
ENST00000509700.1:n.462+386G>T
|
|
|
NM_002241.4:c.1085G>T
|
NP_002232.2:p.Arg362Met
|
|
NM_002241.5:c.1085G>T
MANE Select
|
NP_002232.2:p.Arg362Met
|
|