ENST00000703783.1:n.1104C>T
|
|
|
ENST00000703785.1:n.1185C>T
|
|
|
ENST00000262464.9:c.4320C>T
MANE Select
|
ENSP00000262464.4:p.Phe1440=
|
|
ENST00000262464.8:c.4320C>T
|
ENSP00000262464.4:p.Phe1440=
|
|
ENST00000507835.5:c.870C>T
|
ENSP00000426839.1:p.Phe290=
|
|
ENST00000508053.5:c.4320C>T
|
ENSP00000424571.1:p.Phe1440=
|
|
ENST00000508989.5:c.4221C>T
|
ENSP00000425596.1:p.Phe1407=
|
|
ENST00000619499.4:c.4317C>T
|
ENSP00000482132.1:p.Phe1439=
|
|
NM_001999.3:c.4320C>T
|
NP_001990.2:p.Phe1440=
|
|
XM_017009228.2:c.4167C>T
|
XP_016864717.1:p.Phe1389=
|
|
NM_001999.4:c.4320C>T
MANE Select
|
NP_001990.2:p.Phe1440=
|
|