ENST00000324071.10:c.1136G>C
MANE Select
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ENSP00000324648.2:p.Gly379Ala
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ENST00000598834.2:c.1160G>C
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ENST00000324071.8:c.1136G>C
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ENSP00000324648.2:p.Gly379Ala
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ENST00000593831.1:c.428G>C
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ENSP00000470582.1:p.Gly143Ala
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ENST00000597612.1:n.631G>C
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NM_000767.4:c.1136G>C
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NP_000758.1:p.Gly379Ala
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XM_005258569.3:c.1136G>C
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XP_005258626.1:p.Gly379Ala
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XM_006723050.2:c.1136G>C
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XP_006723113.1:p.Gly379Ala
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XM_011526546.1:c.1136G>C
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XP_011524848.1:p.Gly379Ala
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XM_011526547.1:c.1136G>C
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XP_011524849.1:p.Gly379Ala
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XM_011526548.1:c.656G>C
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XP_011524850.1:p.Gly219Ala
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XM_011526549.1:c.545G>C
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XP_011524851.1:p.Gly182Ala
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XM_011526550.1:c.536G>C
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XP_011524852.1:p.Gly179Ala
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NM_000767.5:c.1136G>C
MANE Select
|
NP_000758.1:p.Gly379Ala
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