ENST00000256084.8:c.3012T=
MANE Select
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ENSP00000256084.7:p.Tyr1004=
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|
ENST00000256084.7:c.3012T=
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ENSP00000256084.7:p.Tyr1004=
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|
ENST00000359874.7:c.3102T=
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ENSP00000352936.3:p.Tyr1034=
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|
NM_001127698.1:c.3102T=
|
NP_001121170.1:p.Tyr1034=
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NM_006846.3:c.3012T= , LRG_110t1:c.3012T=
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NP_006837.2:p.Tyr1004=
|
|
XM_011537550.1:c.3045T=
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XP_011535852.1:p.Tyr1015=
|
|
XM_011537551.1:c.3018T=
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XP_011535853.1:p.Tyr1006=
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|
XM_011537551.2:c.3018T=
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XP_011535853.1:p.Tyr1006=
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|
NM_001127698.2:c.3102T=
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NP_001121170.1:p.Tyr1034=
|
|
NM_006846.4:c.3012T=
MANE Select
|
NP_006837.2:p.Tyr1004=
|
|