ENST00000703783.1:n.1099G>T
|
|
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ENST00000703785.1:n.1180G>T
|
|
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ENST00000262464.9:c.4315G>T
MANE Select
|
ENSP00000262464.4:p.Gly1439Cys
|
|
ENST00000262464.8:c.4315G>T
|
ENSP00000262464.4:p.Gly1439Cys
|
|
ENST00000507835.5:c.865G>T
|
ENSP00000426839.1:p.Gly289Cys
|
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ENST00000508053.5:c.4315G>T
|
ENSP00000424571.1:p.Gly1439Cys
|
|
ENST00000508989.5:c.4216G>T
|
ENSP00000425596.1:p.Gly1406Cys
|
|
ENST00000619499.4:c.4312G>T
|
ENSP00000482132.1:p.Gly1438Cys
|
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NM_001999.3:c.4315G>T
|
NP_001990.2:p.Gly1439Cys
|
|
XM_017009228.2:c.4162G>T
|
XP_016864717.1:p.Gly1388Cys
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|
NM_001999.4:c.4315G>T
MANE Select
|
NP_001990.2:p.Gly1439Cys
|
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