ENST00000474174.2:n.297A=
|
|
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ENST00000698625.1:c.1053A=
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ENSP00000513844.1:p.Pro351=
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|
ENST00000698626.1:c.1053A=
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ENSP00000513845.1:p.Pro351=
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ENST00000698635.1:c.1053A=
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ENSP00000513850.1:p.Pro351=
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|
ENST00000376701.5:c.1053A=
MANE Select
|
ENSP00000365891.4:p.Pro351=
|
|
ENST00000376701.4:c.1053A=
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ENSP00000365891.4:p.Pro351=
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|
ENST00000474174.1:n.297A=
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|
|
NM_000377.2:c.1053A= , LRG_125t1:c.1053A=
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NP_000368.1:p.Pro351=
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|
XM_011543977.1:c.932-35A=
|
XP_011542279.1:n.932-35A=
|
|
XM_011543977.2:c.932-35A=
|
XP_011542279.1:n.932-35A=
|
|
XM_017029786.1:c.1053A=
|
XP_016885275.1:p.Pro351=
|
|
NM_000377.3:c.1053A=
MANE Select
|
NP_000368.1:p.Pro351=
|
|