ENST00000299314.12:c.119T>G
MANE Select
|
ENSP00000299314.7:p.Val40Gly
|
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ENST00000647144.1:n.239T>G
|
|
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ENST00000299314.11:c.119T>G
|
ENSP00000299314.7:p.Val40Gly
|
|
ENST00000392919.4:c.119T>G
|
ENSP00000376651.4:p.Val40Gly
|
|
ENST00000549165.1:c.119T>G
|
ENSP00000450413.1:p.Val40Gly
|
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ENST00000549940.5:c.119T>G
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ENSP00000449150.1:p.Val40Gly
|
|
NM_024312.4:c.119T>G
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NP_077288.2:p.Val40Gly
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XM_006719593.2:c.119T>G
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XP_006719656.1:p.Val40Gly
|
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XM_011538731.1:c.38T>G
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XP_011537033.1:p.Val13Gly
|
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XM_006719593.3:c.119T>G
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XP_006719656.1:p.Val40Gly
|
|
XM_011538731.2:c.38T>G
|
XP_011537033.1:p.Val13Gly
|
|
XM_017019961.1:c.-98T>G
|
XP_016875450.1:n.-98T>G
|
|
XM_017019962.2:c.-1232T>G
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XP_016875451.1:n.-1232T>G
|
|
NM_024312.5:c.119T>G
MANE Select
|
NP_077288.2:p.Val40Gly
|
|