ENST00000307998.11:c.728-1G>T
MANE Select
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ENSP00000309953.6:n.728-1G>T
|
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ENST00000307998.10:c.728-1G>T
|
ENSP00000309953.6:n.728-1G>T
|
|
ENST00000526628.5:n.1293G>T
|
|
|
ENST00000527969.1:n.1412G>T
|
|
|
ENST00000528176.5:c.728-1G>T
|
ENSP00000434151.1:n.728-1G>T
|
|
ENST00000531005.5:n.1722-1G>T
|
|
|
ENST00000531972.5:c.728-1G>T
|
ENSP00000435295.1:n.728-1G>T
|
|
ENST00000532084.5:n.154-1G>T
|
|
|
NM_016938.4:c.728-1G>T
|
NP_058634.4:n.728-1G>T
|
|
NR_037718.1:n.987-1G>T
|
|
|
NM_016938.5:c.728-1G>T
MANE Select
|
NP_058634.4:n.728-1G>T
|
|
NR_037718.2:n.853-1G>T
|
|
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