ENST00000394867.9:n.840A=
|
|
|
ENST00000687128.1:n.840A=
|
|
|
ENST00000262948.10:c.401A=
MANE Select
|
ENSP00000262948.4:p.Tyr134=
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|
ENST00000262948.9:c.401A=
|
ENSP00000262948.3:p.Tyr134=
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|
ENST00000394867.8:c.110A=
|
ENSP00000378336.1:p.Tyr37=
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|
ENST00000599345.1:n.598A=
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|
|
NM_030662.3:c.401A= , LRG_750t1:c.401A=
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NP_109587.1:p.Tyr134=
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|
XM_006722799.2:c.401A=
|
XP_006722862.1:p.Tyr134=
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|
XM_017026989.1:c.401A=
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XP_016882478.1:p.Tyr134=
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|
XM_017026990.1:c.401A=
|
XP_016882479.1:p.Tyr134=
|
|
XM_017026991.1:c.401A=
|
XP_016882480.1:p.Tyr134=
|
|
NM_030662.4:c.401A=
MANE Select
|
NP_109587.1:p.Tyr134=
|
|