ENST00000326003.7:c.447G>A
MANE Select
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ENSP00000314151.1:p.Gly149=
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ENST00000326003.6:c.447G>A
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ENSP00000314151.1:p.Gly149=
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ENST00000360617.7:c.447G>A
|
ENSP00000353829.2:p.Gly149=
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ENST00000422986.6:c.*103G>A
|
ENSP00000393628.2:n.*103G>A
|
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ENST00000593997.5:c.447G>A
|
ENSP00000472907.1:p.Gly149=
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ENST00000595392.5:c.353-30G>A
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ENSP00000468912.1:n.353-30G>A
|
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ENST00000595952.5:c.318G>A
|
ENSP00000471155.1:p.Gly106=
|
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ENST00000596185.5:c.*555G>A
|
ENSP00000471648.1:n.*555G>A
|
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ENST00000596333.1:n.482G>A
|
|
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ENST00000597286.5:c.336G>A
|
ENSP00000470523.1:p.Gly112=
|
|
ENST00000597483.5:c.318G>A
|
ENSP00000472411.1:p.Gly106=
|
|
ENST00000598145.1:c.431G>A
|
|
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ENST00000601349.5:n.1726G>A
|
|
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ENST00000601503.5:c.390G>A
|
ENSP00000472213.1:p.Gly130=
|
|
ENST00000601812.1:n.879G>A
|
|
|
ENST00000617027.4:c.354-30G>A
|
ENSP00000483513.1:n.354-30G>A
|
|
NM_001030047.1:c.447G>A
|
NP_001025218.1:p.Gly149=
|
|
NM_001030048.1:c.318G>A
|
NP_001025219.1:p.Gly106=
|
|
NM_001648.2:c.447G>A
MANE Select
|
NP_001639.1:p.Gly149=
|
|
XM_011526923.1:c.447G>A
|
XP_011525225.1:p.Gly149=
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|
XM_011526924.1:c.447G>A
|
XP_011525226.1:p.Gly149=
|
|
XR_935817.1:n.482G>A
|
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