ENST00000593677.2:c.1065C=
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ENST00000688602.1:c.2462C=
|
|
|
ENST00000689936.1:c.2434C=
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|
|
ENST00000359596.8:c.14129C=
MANE Select
|
ENSP00000352608.2:p.Pro4710=
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ENST00000355481.8:c.14114C=
|
ENSP00000347667.3:p.Pro4705=
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ENST00000359596.7:c.14129C=
|
ENSP00000352608.2:p.Pro4710=
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ENST00000360985.7:c.14111C=
|
ENSP00000354254.4:p.Pro4704=
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NM_000540.2:c.14129C= , LRG_766t1:c.14129C=
|
NP_000531.2:p.Pro4710=
|
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NM_001042723.1:c.14114C=
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NP_001036188.1:p.Pro4705=
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XM_006723317.1:c.14111C=
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XP_006723380.1:p.Pro4704=
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XM_006723319.1:c.14096C=
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XP_006723382.1:p.Pro4699=
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XM_011527204.1:c.14126C=
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XP_011525506.1:p.Pro4709=
|
|
XM_011527205.1:c.14042C=
|
XP_011525507.1:p.Pro4681=
|
|
XM_006723317.2:c.14111C=
|
XP_006723380.1:p.Pro4704=
|
|
XM_006723319.2:c.14096C=
|
XP_006723382.1:p.Pro4699=
|
|
XM_011527205.2:c.14042C=
|
XP_011525507.1:p.Pro4681=
|
|
NM_000540.3:c.14129C=
MANE Select
|
NP_000531.2:p.Pro4710=
|
|
NM_001042723.2:c.14114C=
|
NP_001036188.1:p.Pro4705=
|
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