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ENST00000251849.9:c.1206T=
MANE Select
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NM_002880.3:c.1206T= , LRG_413t1:c.1206T=
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XP_005265412.1:p.His402=
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XM_011533974.1:c.1206T=
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NM_001354692.2:c.963T=
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NP_001341621.1:p.His321=
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NM_001354693.2:c.1107T=
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NP_001341622.1:p.His369=
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NM_001354695.2:c.864T=
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NM_001354690.3:c.1206T=
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NP_001341620.1:p.His321=
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NM_001354692.3:c.963T=
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NP_001341621.1:p.His321=
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NM_001354693.3:c.1107T=
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NP_001341622.1:p.His369=
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NM_001354694.3:c.1023T=
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NP_001341623.1:p.His341=
|
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|
NM_001354695.3:c.864T=
|
NP_001341624.1:p.His288=
|
|
|
NM_002880.4:c.1206T=
MANE Select
|
NP_002871.1:p.His402=
|
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|
NR_148940.3:n.1650T=
|
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NR_148941.3:n.1596T=
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NR_148942.3:n.1535T=
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