ENST00000307998.11:c.974+47G>T
MANE Select
|
ENSP00000309953.6:n.974+47G>T
|
|
ENST00000307998.10:c.974+47G>T
|
ENSP00000309953.6:n.974+47G>T
|
|
ENST00000525392.1:n.135+47G>T
|
|
|
ENST00000526628.5:n.1540+47G>T
|
|
|
ENST00000528176.5:c.974+47G>T
|
ENSP00000434151.1:n.974+47G>T
|
|
ENST00000528409.1:n.207+58G>T
|
|
|
ENST00000530806.5:c.-25+47G>T
|
ENSP00000436526.1:n.-25+47G>T
|
|
ENST00000531005.5:n.1968+47G>T
|
|
|
ENST00000531645.5:c.122+47G>T
|
ENSP00000436521.1:n.122+47G>T
|
|
ENST00000531972.5:c.974+47G>T
|
ENSP00000435295.1:n.974+47G>T
|
|
ENST00000532084.5:n.400+47G>T
|
|
|
NM_016938.4:c.974+47G>T
|
NP_058634.4:n.974+47G>T
|
|
NR_037718.1:n.1233+47G>T
|
|
|
NM_016938.5:c.974+47G>T
MANE Select
|
NP_058634.4:n.974+47G>T
|
|
NR_037718.2:n.1099+47G>T
|
|
|