ENST00000261716.8:c.999+145G>T
MANE Select
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ENSP00000261716.3:n.999+145G>T
|
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ENST00000261716.7:c.999+145G>T
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ENSP00000261716.3:n.999+145G>T
|
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ENST00000536202.1:c.999+145G>T
|
ENSP00000438819.1:n.999+145G>T
|
|
ENST00000577583.1:n.847+145G>T
|
|
|
NM_020791.2:c.999+145G>T
|
NP_065842.1:n.999+145G>T
|
|
NM_025142.1:c.999+145G>T
|
NP_079418.1:n.999+145G>T
|
|
XM_011525060.1:c.999+145G>T
|
XP_011523362.1:n.999+145G>T
|
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XM_011525060.2:c.999+145G>T
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XP_011523362.1:n.999+145G>T
|
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NM_020791.4:c.999+145G>T
MANE Select
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NP_065842.1:n.999+145G>T
|
|