ENST00000299314.12:c.438A>T
MANE Select
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ENSP00000299314.7:p.Pro146=
|
|
ENST00000299314.11:c.438A>T
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ENSP00000299314.7:p.Pro146=
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ENST00000549940.5:c.438A>T
|
ENSP00000449150.1:p.Pro146=
|
|
ENST00000550352.1:n.232A>T
|
|
|
ENST00000552681.1:c.72A>T
|
ENSP00000449217.1:p.Pro24=
|
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NM_024312.4:c.438A>T
|
NP_077288.2:p.Pro146=
|
|
XM_006719593.2:c.438A>T
|
XP_006719656.1:p.Pro146=
|
|
XM_011538731.1:c.357A>T
|
XP_011537033.1:p.Pro119=
|
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XM_006719593.3:c.438A>T
|
XP_006719656.1:p.Pro146=
|
|
XM_011538731.2:c.357A>T
|
XP_011537033.1:p.Pro119=
|
|
XM_017019961.1:c.222A>T
|
XP_016875450.1:p.Pro74=
|
|
XM_017019962.2:c.-913A>T
|
XP_016875451.1:n.-913A>T
|
|
NM_024312.5:c.438A>T
MANE Select
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NP_077288.2:p.Pro146=
|
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