ENST00000261208.8:c.822G>A
MANE Select
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ENSP00000261208.3:p.Trp274Ter
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|
ENST00000261208.7:c.822G>A
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ENSP00000261208.3:p.Trp274Ter
|
|
ENST00000538703.5:c.822G>A
|
ENSP00000440861.1:p.Trp274Ter
|
|
ENST00000541929.5:c.198G>A
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ENSP00000446364.1:p.Trp66Ter
|
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ENST00000544080.6:c.*251G>A
|
ENSP00000439385.2:n.*251G>A
|
|
ENST00000546999.5:c.*251G>A
|
ENSP00000447675.1:n.*251G>A
|
|
ENST00000549376.1:n.215G>A
|
|
|
ENST00000551562.1:n.82G>A
|
|
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ENST00000552509.5:c.786G>A
|
ENSP00000450372.1:p.Trp262Ter
|
|
NM_001258333.1:c.198G>A
|
NP_001245262.1:p.Trp66Ter
|
|
NM_001258334.1:c.822G>A
|
NP_001245263.1:p.Trp274Ter
|
|
NM_002108.3:c.822G>A
|
NP_002099.1:p.Trp274Ter
|
|
XM_011538249.1:c.4-2186G>A
|
XP_011536551.1:n.4-2186G>A
|
|
XM_011538249.2:c.4-2186G>A
|
XP_011536551.1:n.4-2186G>A
|
|
NM_002108.4:c.822G>A
MANE Select
|
NP_002099.1:p.Trp274Ter
|
|
NM_001258334.2:c.822G>A
|
NP_001245263.1:p.Trp274Ter
|
|
NM_001258333.2:c.198G>A
|
NP_001245262.1:p.Trp66Ter
|
|