ENST00000703783.1:n.655C=
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|
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ENST00000703785.1:n.736C=
|
|
|
ENST00000262464.9:c.3871C=
MANE Select
|
ENSP00000262464.4:p.Pro1291=
|
|
ENST00000262464.8:c.3871C=
|
ENSP00000262464.4:p.Pro1291=
|
|
ENST00000507835.5:c.421C=
|
ENSP00000426839.1:p.Pro141=
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|
ENST00000508053.5:c.3871C=
|
ENSP00000424571.1:p.Pro1291=
|
|
ENST00000508989.5:c.3772C=
|
ENSP00000425596.1:p.Pro1258=
|
|
ENST00000619499.4:c.3868C=
|
ENSP00000482132.1:p.Pro1290=
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|
NM_001999.3:c.3871C=
|
NP_001990.2:p.Pro1291=
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|
XM_017009228.2:c.3718C=
|
XP_016864717.1:p.Pro1240=
|
|
NM_001999.4:c.3871C=
MANE Select
|
NP_001990.2:p.Pro1291=
|
|