ENST00000703783.1:n.976G>A
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|
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ENST00000703785.1:n.1057G>A
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|
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ENST00000262464.9:c.4192G>A
MANE Select
|
ENSP00000262464.4:p.Gly1398Ser
|
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ENST00000262464.8:c.4192G>A
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ENSP00000262464.4:p.Gly1398Ser
|
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ENST00000507835.5:c.742G>A
|
ENSP00000426839.1:p.Gly248Ser
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ENST00000508053.5:c.4192G>A
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ENSP00000424571.1:p.Gly1398Ser
|
|
ENST00000508989.5:c.4093G>A
|
ENSP00000425596.1:p.Gly1365Ser
|
|
ENST00000619499.4:c.4189G>A
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ENSP00000482132.1:p.Gly1397Ser
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NM_001999.3:c.4192G>A
|
NP_001990.2:p.Gly1398Ser
|
|
XM_017009228.2:c.4039G>A
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XP_016864717.1:p.Gly1347Ser
|
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NM_001999.4:c.4192G>A
MANE Select
|
NP_001990.2:p.Gly1398Ser
|
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