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ENST00000337432.9:c.606T=
MANE Select
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ENSP00000336701.4:p.Asp202=
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NM_058216.2:c.606T=
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NR_103872.1:n.510T=
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XM_006722001.2:c.606T=
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XM_006722002.2:c.606T=
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XP_006722065.1:p.Asp202=
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XM_006722005.2:c.255T=
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XM_011525092.1:c.255T=
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XM_011525093.1:c.255T=
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XM_011525094.1:c.255T=
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XR_934514.1:n.679T=
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XM_006722001.4:c.606T=
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XM_006722002.4:c.606T=
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XP_006722065.1:p.Asp202=
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XM_006722004.3:c.255T=
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XM_006722005.3:c.255T=
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XP_006722068.1:p.Asp85=
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XM_011525092.2:c.255T=
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XP_011523394.1:p.Asp85=
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XM_011525093.2:c.255T=
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XP_011523395.1:p.Asp85=
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XM_011525094.2:c.255T=
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XP_011523396.1:p.Asp85=
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XM_017024914.1:c.255T=
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XP_016880403.1:p.Asp85=
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XM_017024915.1:c.255T=
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XM_017024916.1:c.255T=
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XP_016880405.1:p.Asp85=
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XM_017024917.1:c.255T=
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XP_016880406.1:p.Asp85=
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XM_017024918.2:c.255T=
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XP_016880407.1:p.Asp85=
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XM_017024919.1:c.255T=
|
XP_016880408.1:p.Asp85=
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XR_934513.3:n.1110T=
|
|
|
|
XR_934514.3:n.1110T=
|
|
|
|
NM_058216.3:c.606T=
MANE Select
|
NP_478123.1:p.Asp202=
|
|
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NR_103872.2:n.481T=
|
|
|
