ENST00000555911.2:c.880G>C
|
ENSP00000452551.2:p.Asp294His
|
|
ENST00000698939.1:c.771-273G>C
|
ENSP00000514047.1:n.771-273G>C
|
|
ENST00000397532.9:c.880G>C
|
ENSP00000380666.4:p.Asp294His
|
|
ENST00000674313.1:c.880G>C
MANE Select
|
ENSP00000501493.1:p.Asp294His
|
|
ENST00000285850.11:c.880G>C
|
ENSP00000285850.7:p.Asp294His
|
|
ENST00000397528.8:c.880G>C
|
ENSP00000380662.4:p.Asp294His
|
|
ENST00000397529.6:c.880G>C
|
ENSP00000380663.2:p.Asp294His
|
|
ENST00000397532.7:c.880G>C
|
ENSP00000380666.3:p.Asp294His
|
|
ENST00000554061.5:n.551G>C
|
|
|
ENST00000554517.5:c.82G>C
|
ENSP00000452083.1:p.Asp28His
|
|
ENST00000555702.5:c.880G>C
|
ENSP00000451881.1:p.Asp294His
|
|
ENST00000556287.5:c.880G>C
|
ENSP00000450715.1:p.Asp294His
|
|
ENST00000556350.1:c.24G>C
|
|
|
NM_001126105.2:c.880G>C , LRG_695t1:c.880G>C
|
NP_001119577.1:p.Asp294His
|
|
NM_001126106.2:c.880G>C , LRG_695t2:c.880G>C
|
NP_001119578.1:p.Asp294His
|
|
NR_040448.1:n.1495G>C
|
|
|
XM_006720302.1:c.880G>C
|
XP_006720365.1:p.Asp294His
|
|
XM_011537298.1:c.880G>C
|
XP_011535600.1:p.Asp294His
|
|
XM_011537299.1:c.880G>C
|
XP_011535601.1:p.Asp294His
|
|
XM_006720302.2:c.880G>C
|
XP_006720365.1:p.Asp294His
|
|
XM_011537298.3:c.880G>C
|
XP_011535600.1:p.Asp294His
|
|
NM_001126105.3:c.880G>C
|
NP_001119577.1:p.Asp294His
|
|
NM_001126106.4:c.880G>C
|
NP_001119578.1:p.Asp294His
|
|
NM_003982.4:c.880G>C
MANE Select
|
NP_003973.3:p.Asp294His
|
|