ENST00000326003.7:c.737T>C
MANE Select
|
ENSP00000314151.1:p.Val246Ala
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|
ENST00000326003.6:c.737T>C
|
ENSP00000314151.1:p.Val246Ala
|
|
ENST00000360617.7:c.1179T>C
|
ENSP00000353829.2:n.1179T>C
|
|
ENST00000422986.6:c.*393T>C
|
ENSP00000393628.2:n.*393T>C
|
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ENST00000595392.5:c.*238T>C
|
ENSP00000468912.1:n.*238T>C
|
|
ENST00000595952.5:c.608T>C
|
ENSP00000471155.1:p.Val203Ala
|
|
ENST00000596333.1:n.915T>C
|
|
|
ENST00000598145.1:c.739T>C
|
|
|
ENST00000601349.5:n.2016T>C
|
|
|
ENST00000601812.1:n.1169T>C
|
|
|
ENST00000617027.4:c.614T>C
|
ENSP00000483513.1:p.Val205Ala
|
|
NM_001030047.1:c.*462T>C
|
NP_001025218.1:n.*462T>C
|
|
NM_001030048.1:c.608T>C
|
NP_001025219.1:p.Val203Ala
|
|
NM_001648.2:c.737T>C
MANE Select
|
NP_001639.1:p.Val246Ala
|
|
XM_011526923.1:c.755T>C
|
XP_011525225.1:p.Val252Ala
|
|
XR_935817.1:n.1324+824T>C
|
|
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