ENST00000697602.1:n.1354C>G
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ENST00000697603.1:c.3458C>G
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ENSP00000513358.1:p.Ala1153Gly
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ENST00000314191.7:c.10781C>G
MANE Select
|
ENSP00000313420.3:p.Ala3594Gly
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ENST00000314191.6:c.10781C>G
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ENSP00000313420.3:p.Ala3594Gly
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ENST00000338368.7:c.10781C>G
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ENSP00000345182.4:p.Ala3594Gly
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NM_001081640.1:c.10781C>G
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NP_001075109.1:p.Ala3594Gly
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NM_006904.6:c.10781C>G , LRG_162t1:c.10781C>G
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NP_008835.5:p.Ala3594Gly
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XM_011517567.1:c.10784C>G
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XP_011515869.1:p.Ala3595Gly
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XM_011517568.1:c.10784C>G
|
XP_011515870.1:p.Ala3595Gly
|
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NM_001081640.2:c.10781C>G
|
NP_001075109.1:p.Ala3594Gly
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NM_006904.7:c.10781C>G
MANE Select
|
NP_008835.5:p.Ala3594Gly
|
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