ENST00000593677.2:c.1184G>T
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|
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ENST00000688602.1:c.2581G>T
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|
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ENST00000689936.1:c.2553G>T
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|
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ENST00000359596.8:c.14248G>T
MANE Select
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ENSP00000352608.2:p.Glu4750Ter
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ENST00000355481.8:c.14233G>T
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ENSP00000347667.3:p.Glu4745Ter
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ENST00000359596.7:c.14248G>T
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ENSP00000352608.2:p.Glu4750Ter
|
|
ENST00000360985.7:c.14230G>T
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ENSP00000354254.4:p.Glu4744Ter
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NM_000540.2:c.14248G>T , LRG_766t1:c.14248G>T
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NP_000531.2:p.Glu4750Ter
|
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NM_001042723.1:c.14233G>T
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NP_001036188.1:p.Glu4745Ter
|
|
XM_006723317.1:c.14230G>T
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XP_006723380.1:p.Glu4744Ter
|
|
XM_006723319.1:c.14215G>T
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XP_006723382.1:p.Glu4739Ter
|
|
XM_011527204.1:c.14245G>T
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XP_011525506.1:p.Glu4749Ter
|
|
XM_011527205.1:c.14161G>T
|
XP_011525507.1:p.Glu4721Ter
|
|
XM_006723317.2:c.14230G>T
|
XP_006723380.1:p.Glu4744Ter
|
|
XM_006723319.2:c.14215G>T
|
XP_006723382.1:p.Glu4739Ter
|
|
XM_011527205.2:c.14161G>T
|
XP_011525507.1:p.Glu4721Ter
|
|
NM_000540.3:c.14248G>T
MANE Select
|
NP_000531.2:p.Glu4750Ter
|
|
NM_001042723.2:c.14233G>T
|
NP_001036188.1:p.Glu4745Ter
|
|