ENST00000508053.6:c.532+67A>C
|
ENSP00000424571.2:n.532+67A>C
|
|
ENST00000703787.1:n.239+67A>C
|
|
|
ENST00000262464.9:c.532+67A>C
MANE Select
|
ENSP00000262464.4:n.532+67A>C
|
|
ENST00000262464.8:c.532+67A>C
|
ENSP00000262464.4:n.532+67A>C
|
|
ENST00000502468.5:c.532+67A>C
|
ENSP00000424753.1:n.532+67A>C
|
|
ENST00000508053.5:c.532+67A>C
|
ENSP00000424571.1:n.532+67A>C
|
|
ENST00000508989.5:c.433+67A>C
|
ENSP00000425596.1:n.433+67A>C
|
|
ENST00000514742.1:n.1152+67A>C
|
|
|
ENST00000619499.4:c.532+67A>C
|
ENSP00000482132.1:n.532+67A>C
|
|
ENST00000620257.1:c.532+67A>C
|
ENSP00000479157.1:n.532+67A>C
|
|
NM_001999.3:c.532+67A>C
|
NP_001990.2:n.532+67A>C
|
|
XM_017009228.2:c.532+67A>C
|
XP_016864717.1:n.532+67A>C
|
|
NM_001999.4:c.532+67A>C
MANE Select
|
NP_001990.2:n.532+67A>C
|
|