ENST00000593677.2:c.1608G>C
|
|
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ENST00000688602.1:c.3005G>C
|
|
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ENST00000689936.1:c.2977G>C
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|
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ENST00000692547.1:n.65G>C
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|
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ENST00000359596.8:c.14672G>C
MANE Select
|
ENSP00000352608.2:p.Gly4891Ala
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ENST00000355481.8:c.14657G>C
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ENSP00000347667.3:p.Gly4886Ala
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|
ENST00000359596.7:c.14672G>C
|
ENSP00000352608.2:p.Gly4891Ala
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ENST00000360985.7:c.14654G>C
|
ENSP00000354254.4:p.Gly4885Ala
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NM_000540.2:c.14672G>C , LRG_766t1:c.14672G>C
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NP_000531.2:p.Gly4891Ala
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NM_001042723.1:c.14657G>C
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NP_001036188.1:p.Gly4886Ala
|
|
XM_006723317.1:c.14654G>C
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XP_006723380.1:p.Gly4885Ala
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|
XM_006723319.1:c.14639G>C
|
XP_006723382.1:p.Gly4880Ala
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XM_011527204.1:c.14669G>C
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XP_011525506.1:p.Gly4890Ala
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|
XM_011527205.1:c.14585G>C
|
XP_011525507.1:p.Gly4862Ala
|
|
XM_006723317.2:c.14654G>C
|
XP_006723380.1:p.Gly4885Ala
|
|
XM_006723319.2:c.14639G>C
|
XP_006723382.1:p.Gly4880Ala
|
|
XM_011527205.2:c.14585G>C
|
XP_011525507.1:p.Gly4862Ala
|
|
NM_000540.3:c.14672G>C
MANE Select
|
NP_000531.2:p.Gly4891Ala
|
|
NM_001042723.2:c.14657G>C
|
NP_001036188.1:p.Gly4886Ala
|
|