ENST00000593677.2:c.1716T>C
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|
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ENST00000688602.1:c.3113T>C
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|
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ENST00000689936.1:c.3085T>C
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|
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ENST00000692547.1:n.173T>C
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|
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ENST00000359596.8:c.14780T>C
MANE Select
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ENSP00000352608.2:p.Val4927Ala
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ENST00000355481.8:c.14765T>C
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ENSP00000347667.3:p.Val4922Ala
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|
ENST00000359596.7:c.14780T>C
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ENSP00000352608.2:p.Val4927Ala
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|
ENST00000360985.7:c.14762T>C
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ENSP00000354254.4:p.Val4921Ala
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NM_000540.2:c.14780T>C , LRG_766t1:c.14780T>C
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NP_000531.2:p.Val4927Ala
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NM_001042723.1:c.14765T>C
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NP_001036188.1:p.Val4922Ala
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|
XM_006723317.1:c.14762T>C
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XP_006723380.1:p.Val4921Ala
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|
XM_006723319.1:c.14747T>C
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XP_006723382.1:p.Val4916Ala
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|
XM_011527204.1:c.14777T>C
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XP_011525506.1:p.Val4926Ala
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|
XM_011527205.1:c.14693T>C
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XP_011525507.1:p.Val4898Ala
|
|
XM_006723317.2:c.14762T>C
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XP_006723380.1:p.Val4921Ala
|
|
XM_006723319.2:c.14747T>C
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XP_006723382.1:p.Val4916Ala
|
|
XM_011527205.2:c.14693T>C
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XP_011525507.1:p.Val4898Ala
|
|
NM_000540.3:c.14780T>C
MANE Select
|
NP_000531.2:p.Val4927Ala
|
|
NM_001042723.2:c.14765T>C
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NP_001036188.1:p.Val4922Ala
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