ENST00000299421.9:c.982G>C
(ILK)
MANE Select
|
ENSP00000299421.4:p.Asp328His
|
|
ENST00000299424.9:c.*983C>G
(TAF10)
MANE Select
|
ENSP00000299424.4:n.*983C>G
|
|
ENST00000299421.8:c.982G>C
(ILK)
|
ENSP00000299421.3:p.Asp328His
|
|
ENST00000396751.6:c.982G>C
(ILK)
|
ENSP00000379975.2:p.Asp328His
|
|
ENST00000420936.6:c.982G>C
(ILK)
|
ENSP00000403487.2:p.Asp328His
|
|
ENST00000526318.2:c.328-664G>C
(ILK)
|
ENSP00000480597.1:n.328-664G>C
|
|
ENST00000526711.5:c.*693G>C
(ILK)
|
ENSP00000479932.1:n.*693G>C
|
|
ENST00000528784.5:n.855G>C
(ILK)
|
|
|
ENST00000528995.5:c.799G>C
(ILK)
|
ENSP00000435323.1:p.Asp267His
|
|
ENST00000530016.5:n.1319G>C
(ILK)
|
|
|
ENST00000532063.5:c.580G>C
(ILK)
|
ENSP00000434492.2:p.Asp194His
|
|
ENST00000537806.5:c.1075G>C
(ILK)
|
ENSP00000439606.2:p.Asp359His
|
|
ENST00000616342.1:n.1749C>G
(TAF10)
|
|
|
NM_001014794.2:c.982G>C
(ILK)
|
NP_001014794.1:p.Asp328His
|
|
NM_001014795.2:c.982G>C
(ILK)
|
NP_001014795.1:p.Asp328His
|
|
NM_001278441.1:c.799G>C
(ILK)
|
NP_001265370.1:p.Asp267His
|
|
NM_001278442.1:c.580G>C
(ILK)
|
NP_001265371.1:p.Asp194His
|
|
NM_004517.3:c.982G>C
(ILK)
|
NP_004508.1:p.Asp328His
|
|
XM_005252904.3:c.982G>C
(ILK)
|
XP_005252961.1:p.Asp328His
|
|
XM_005252905.1:c.580G>C
(ILK)
|
XP_005252962.1:p.Asp194His
|
|
XM_011520065.1:c.982G>C
(ILK)
|
XP_011518367.1:p.Asp328His
|
|
XM_005252904.5:c.982G>C
(ILK)
|
XP_005252961.1:p.Asp328His
|
|
XM_005252905.3:c.580G>C
(ILK)
|
XP_005252962.1:p.Asp194His
|
|
XM_017017672.1:c.829G>C
(ILK)
|
XP_016873161.1:p.Asp277His
|
|
XM_024448494.1:c.1075G>C
(ILK)
|
XP_024304262.1:p.Asp359His
|
|
XM_024448495.1:c.1075G>C
(ILK)
|
XP_024304263.1:p.Asp359His
|
|
XM_024448496.1:c.1075G>C
(ILK)
|
XP_024304264.1:p.Asp359His
|
|
XM_024448497.1:c.1075G>C
(ILK)
|
XP_024304265.1:p.Asp359His
|
|
XM_024448498.1:c.829G>C
(ILK)
|
XP_024304266.1:p.Asp277His
|
|
XM_024448499.1:c.829G>C
(ILK)
|
XP_024304267.1:p.Asp277His
|
|
XM_024448500.1:c.673G>C
(ILK)
|
XP_024304268.1:p.Asp225His
|
|
NM_006284.4:c.*983C>G
(TAF10)
MANE Select
|
NP_006275.1:n.*983C>G
|
|
NM_001014794.3:c.982G>C
(ILK)
|
NP_001014794.1:p.Asp328His
|
|
NM_001014795.3:c.982G>C
(ILK)
|
NP_001014795.1:p.Asp328His
|
|
NM_001278441.2:c.799G>C
(ILK)
|
NP_001265370.1:p.Asp267His
|
|
NM_004517.4:c.982G>C
(ILK)
MANE Select
|
NP_004508.1:p.Asp328His
|
|
NM_001278442.2:c.580G>C
(ILK)
|
NP_001265371.1:p.Asp194His
|
|