ENST00000216373.10:c.436G>T
MANE Select
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ENSP00000216373.5:p.Gly146Cys
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ENST00000216373.9:c.436G>T
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ENSP00000216373.5:p.Gly146Cys
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|
ENST00000543680.5:c.436G>T
|
ENSP00000445328.1:p.Gly146Cys
|
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ENST00000555666.1:n.615G>T
|
|
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ENST00000556469.5:n.407G>T
|
|
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NM_006939.2:c.436G>T
|
NP_008870.2:p.Gly146Cys
|
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XM_005268021.1:c.256G>T
|
XP_005268078.1:p.Gly86Cys
|
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XM_011537103.1:c.397G>T
|
XP_011535405.1:p.Gly133Cys
|
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XM_011537104.1:c.436G>T
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XP_011535406.1:p.Gly146Cys
|
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XR_943842.1:n.1039+15893C>A
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|
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XR_943843.1:n.1039+15893C>A
|
|
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NM_006939.3:c.436G>T
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NP_008870.2:p.Gly146Cys
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|
NM_006939.4:c.436G>T
MANE Select
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NP_008870.2:p.Gly146Cys
|
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