ENST00000333360.12:c.529+270G=
(SELE)
MANE Select
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ENSP00000331736.7:n.529+270G=
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ENST00000333360.11:c.529+270G=
(SELE)
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ENSP00000331736.7:n.529+270G=
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ENST00000367774.1:c.529+270G=
(SELE)
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ENSP00000356748.1:n.529+270G=
|
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ENST00000367775.5:c.529+270G=
(SELE)
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ENSP00000356749.1:n.529+270G=
|
|
ENST00000367776.5:c.529+270G=
(SELE)
|
ENSP00000356750.1:n.529+270G=
|
|
ENST00000367777.5:c.529+270G=
(SELE)
|
ENSP00000356751.1:n.529+270G=
|
|
ENST00000461085.1:n.482G=
(SELE)
|
|
|
ENST00000498289.5:n.851+47633C=
(FIRRM)
|
|
|
NM_000450.2:c.529+270G=
(SELE)
MANE Select
|
NP_000441.2:n.529+270G=
|
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