ENST00000309383.6:c.2132C>G
MANE Select
|
ENSP00000310649.1:p.Ala711Gly
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ENST00000309383.5:c.2132C>G
|
ENSP00000310649.1:p.Ala711Gly
|
|
ENST00000326848.7:c.1217C>G
|
ENSP00000320853.7:p.Ala406Gly
|
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ENST00000590333.5:c.2180C>G
|
ENSP00000468190.1:p.Ala727Gly
|
|
NM_032430.1:c.2132C>G
|
NP_115806.1:p.Ala711Gly
|
|
XM_005259327.2:c.1862C>G
|
XP_005259384.1:p.Ala621Gly
|
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XM_011527395.1:c.1889C>G
|
XP_011525697.1:p.Ala630Gly
|
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XR_430213.2:n.2115C>G
|
|
|
XM_005259327.3:c.1862C>G
|
XP_005259384.1:p.Ala621Gly
|
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XM_011527395.2:c.1604C>G
|
XP_011525697.2:p.Ala535Gly
|
|
XM_024451739.1:c.1907C>G
|
XP_024307507.1:p.Ala636Gly
|
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XR_430213.4:n.2413C>G
|
|
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NM_032430.2:c.2132C>G
MANE Select
|
NP_115806.1:p.Ala711Gly
|
|