ENST00000703783.1:n.618G>C
|
|
|
ENST00000703785.1:n.699G>C
|
|
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ENST00000262464.9:c.3834G>C
MANE Select
|
ENSP00000262464.4:p.Gly1278=
|
|
ENST00000262464.8:c.3834G>C
|
ENSP00000262464.4:p.Gly1278=
|
|
ENST00000507835.5:c.384G>C
|
ENSP00000426839.1:p.Gly128=
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|
ENST00000508053.5:c.3834G>C
|
ENSP00000424571.1:p.Gly1278=
|
|
ENST00000508989.5:c.3735G>C
|
ENSP00000425596.1:p.Gly1245=
|
|
ENST00000619499.4:c.3831G>C
|
ENSP00000482132.1:p.Gly1277=
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|
NM_001999.3:c.3834G>C
|
NP_001990.2:p.Gly1278=
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|
XM_017009228.2:c.3681G>C
|
XP_016864717.1:p.Gly1227=
|
|
NM_001999.4:c.3834G>C
MANE Select
|
NP_001990.2:p.Gly1278=
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|