ENST00000681320.1:c.8042C=
MANE Select
|
ENSP00000506558.1:p.Pro2681=
|
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ENST00000328333.12:c.8042C=
|
ENSP00000332371.8:p.Pro2681=
|
|
ENST00000487017.5:n.4681C=
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|
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NM_000094.3:c.8042C= , LRG_286t1:c.8042C=
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NP_000085.1:p.Pro2681=
|
|
XM_011533336.1:c.8069C=
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XP_011531638.1:p.Pro2690=
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|
XM_011533337.1:c.8042C=
|
XP_011531639.1:p.Pro2681=
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|
XM_011533338.1:c.8009C=
|
XP_011531640.1:p.Pro2670=
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XR_940369.1:n.8105C=
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|
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XR_940370.1:n.8105C=
|
|
|
XR_940371.1:n.8105C=
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|
|
XM_017005688.1:c.7982C=
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XP_016861177.1:p.Pro2661=
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|
XR_001740003.1:n.8078C=
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|
|
XR_001740004.1:n.8078C=
|
|
|
XR_001740005.1:n.8078C=
|
|
|
NM_000094.4:c.8042C=
MANE Select
|
NP_000085.1:p.Pro2681=
|
|