ENST00000593677.2:c.1343G>T
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|
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ENST00000688602.1:c.2740G>T
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|
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ENST00000689936.1:c.2712G>T
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|
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ENST00000359596.8:c.14407G>T
MANE Select
|
ENSP00000352608.2:p.Gly4803Ter
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|
ENST00000355481.8:c.14392G>T
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ENSP00000347667.3:p.Gly4798Ter
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|
ENST00000359596.7:c.14407G>T
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ENSP00000352608.2:p.Gly4803Ter
|
|
ENST00000360985.7:c.14389G>T
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ENSP00000354254.4:p.Gly4797Ter
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NM_000540.2:c.14407G>T , LRG_766t1:c.14407G>T
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NP_000531.2:p.Gly4803Ter
|
|
NM_001042723.1:c.14392G>T
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NP_001036188.1:p.Gly4798Ter
|
|
XM_006723317.1:c.14389G>T
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XP_006723380.1:p.Gly4797Ter
|
|
XM_006723319.1:c.14374G>T
|
XP_006723382.1:p.Gly4792Ter
|
|
XM_011527204.1:c.14404G>T
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XP_011525506.1:p.Gly4802Ter
|
|
XM_011527205.1:c.14320G>T
|
XP_011525507.1:p.Gly4774Ter
|
|
XM_006723317.2:c.14389G>T
|
XP_006723380.1:p.Gly4797Ter
|
|
XM_006723319.2:c.14374G>T
|
XP_006723382.1:p.Gly4792Ter
|
|
XM_011527205.2:c.14320G>T
|
XP_011525507.1:p.Gly4774Ter
|
|
NM_000540.3:c.14407G>T
MANE Select
|
NP_000531.2:p.Gly4803Ter
|
|
NM_001042723.2:c.14392G>T
|
NP_001036188.1:p.Gly4798Ter
|
|