ENST00000326003.7:c.405T>C
MANE Select
|
ENSP00000314151.1:p.Ala135=
|
|
ENST00000326003.6:c.405T>C
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ENSP00000314151.1:p.Ala135=
|
|
ENST00000360617.7:c.405T>C
|
ENSP00000353829.2:p.Ala135=
|
|
ENST00000422986.6:c.*61T>C
|
ENSP00000393628.2:n.*61T>C
|
|
ENST00000593997.5:c.405T>C
|
ENSP00000472907.1:p.Ala135=
|
|
ENST00000595392.5:c.352+53T>C
|
ENSP00000468912.1:n.352+53T>C
|
|
ENST00000595952.5:c.276T>C
|
ENSP00000471155.1:p.Ala92=
|
|
ENST00000596185.5:c.*513T>C
|
ENSP00000471648.1:n.*513T>C
|
|
ENST00000596333.1:n.440T>C
|
|
|
ENST00000597286.5:c.294T>C
|
ENSP00000470523.1:p.Ala98=
|
|
ENST00000597483.5:c.276T>C
|
ENSP00000472411.1:p.Ala92=
|
|
ENST00000598145.1:c.389T>C
|
|
|
ENST00000601349.5:n.1684T>C
|
|
|
ENST00000601503.5:c.348T>C
|
ENSP00000472213.1:p.Ala116=
|
|
ENST00000601812.1:n.837T>C
|
|
|
ENST00000617027.4:c.353+52T>C
|
ENSP00000483513.1:n.353+52T>C
|
|
NM_001030047.1:c.405T>C
|
NP_001025218.1:p.Ala135=
|
|
NM_001030048.1:c.276T>C
|
NP_001025219.1:p.Ala92=
|
|
NM_001648.2:c.405T>C
MANE Select
|
NP_001639.1:p.Ala135=
|
|
XM_011526923.1:c.405T>C
|
XP_011525225.1:p.Ala135=
|
|
XM_011526924.1:c.405T>C
|
XP_011525226.1:p.Ala135=
|
|
XR_935817.1:n.440T>C
|
|
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