ENST00000324041.6:c.501C>A
MANE Select
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ENSP00000326159.1:p.Cys167Ter
|
|
ENST00000324041.5:c.501C>A
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ENSP00000326159.1:p.Cys167Ter
|
|
ENST00000431178.2:c.328+109C>A
|
ENSP00000399448.2:n.328+109C>A
|
|
ENST00000593885.1:c.212C>A
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ENSP00000469769.1:p.Ala71Glu
|
|
ENST00000596876.1:n.503C>A
|
|
|
ENST00000598305.5:c.212C>A
|
ENSP00000469963.1:p.Ala71Glu
|
|
ENST00000599865.5:n.437C>A
|
|
|
ENST00000602148.1:c.513C>A
|
ENSP00000472091.1:n.513C>A
|
|
NM_001302961.1:c.216C>A
|
NP_001289890.1:p.Cys72Ter
|
|
NM_004917.4:c.501C>A
|
NP_004908.4:p.Cys167Ter
|
|
NR_126566.1:n.490C>A
|
|
|
XM_005259441.3:c.216C>A
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XP_005259498.2:p.Cys72Ter
|
|
XM_011527545.1:c.497C>A
|
XP_011525847.1:p.Ala166Glu
|
|
XM_011527546.1:c.475+109C>A
|
XP_011525848.1:n.475+109C>A
|
|
XM_011527547.1:c.354C>A
|
XP_011525849.1:p.Cys118Ter
|
|
XM_005259441.4:c.216C>A
|
XP_005259498.2:p.Cys72Ter
|
|
XM_011527545.3:c.497C>A
|
XP_011525847.1:p.Ala166Glu
|
|
XM_011527546.2:c.475+109C>A
|
XP_011525848.1:n.475+109C>A
|
|
NM_001302961.2:c.216C>A
|
NP_001289890.1:p.Cys72Ter
|
|
NR_126566.2:n.490C>A
|
|
|
NM_004917.5:c.501C>A
MANE Select
|
NP_004908.4:p.Cys167Ter
|
|