ENST00000326003.7:c.362T>A
MANE Select
|
ENSP00000314151.1:p.Leu121His
|
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ENST00000326003.6:c.362T>A
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ENSP00000314151.1:p.Leu121His
|
|
ENST00000360617.7:c.362T>A
|
ENSP00000353829.2:p.Leu121His
|
|
ENST00000422986.6:c.*18T>A
|
ENSP00000393628.2:n.*18T>A
|
|
ENST00000593997.5:c.362T>A
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ENSP00000472907.1:p.Leu121His
|
|
ENST00000595392.5:c.352+10T>A
|
ENSP00000468912.1:n.352+10T>A
|
|
ENST00000595952.5:c.233T>A
|
ENSP00000471155.1:p.Leu78His
|
|
ENST00000596185.5:c.*470T>A
|
ENSP00000471648.1:n.*470T>A
|
|
ENST00000596333.1:n.397T>A
|
|
|
ENST00000597286.5:c.251T>A
|
ENSP00000470523.1:p.Leu84His
|
|
ENST00000597483.5:c.233T>A
|
ENSP00000472411.1:p.Leu78His
|
|
ENST00000598145.1:c.346T>A
|
|
|
ENST00000601349.5:n.1641T>A
|
|
|
ENST00000601503.5:c.305T>A
|
ENSP00000472213.1:p.Leu102His
|
|
ENST00000601812.1:n.794T>A
|
|
|
ENST00000617027.4:c.353+9T>A
|
ENSP00000483513.1:n.353+9T>A
|
|
NM_001030047.1:c.362T>A
|
NP_001025218.1:p.Leu121His
|
|
NM_001030048.1:c.233T>A
|
NP_001025219.1:p.Leu78His
|
|
NM_001648.2:c.362T>A
MANE Select
|
NP_001639.1:p.Leu121His
|
|
XM_011526923.1:c.362T>A
|
XP_011525225.1:p.Leu121His
|
|
XM_011526924.1:c.362T>A
|
XP_011525226.1:p.Leu121His
|
|
XR_935817.1:n.397T>A
|
|
|