ENST00000684145.1:c.-34T>C
|
ENSP00000508396.1:n.-34T>C
|
|
ENST00000410087.8:c.723T>C
MANE Select
|
ENSP00000386725.3:p.His241=
|
|
ENST00000339098.9:c.801T>C
|
ENSP00000341159.5:p.His267=
|
|
ENST00000374967.6:c.659T>C
|
ENSP00000364106.2:n.659T>C
|
|
ENST00000374969.6:c.482-8955T>C
|
ENSP00000364108.2:n.482-8955T>C
|
|
ENST00000374970.6:c.614-8955T>C
|
ENSP00000364109.2:n.614-8955T>C
|
|
ENST00000409440.7:c.669T>C
|
ENSP00000387080.3:p.His223=
|
|
ENST00000410087.7:c.723T>C
|
ENSP00000386725.3:p.His241=
|
|
ENST00000421817.5:c.*5T>C
|
ENSP00000411466.1:n.*5T>C
|
|
ENST00000452174.5:c.527T>C
|
ENSP00000409198.1:n.527T>C
|
|
ENST00000466715.5:n.539T>C
|
|
|
ENST00000479558.5:n.721T>C
|
|
|
ENST00000494398.5:n.723T>C
|
|
|
NM_001030311.2:c.801T>C
|
NP_001025482.1:p.His267=
|
|
NM_001030312.2:c.482-8955T>C
|
NP_001025483.1:n.482-8955T>C
|
|
NM_001030313.2:c.614-8955T>C
|
NP_001025484.1:n.614-8955T>C
|
|
NM_001160277.1:c.669T>C
|
NP_001153749.1:p.His223=
|
|
NM_201548.4:c.723T>C
|
NP_963842.1:p.His241=
|
|
NR_027689.1:n.628T>C
|
|
|
NR_027690.1:n.760T>C
|
|
|
NM_201548.5:c.723T>C
MANE Select
|
NP_963842.1:p.His241=
|
|
NM_001030311.3:c.801T>C
|
NP_001025482.1:p.His267=
|
|
NM_001030312.3:c.482-8955T>C
|
NP_001025483.1:n.482-8955T>C
|
|
NM_001030313.3:c.614-8955T>C
|
NP_001025484.1:n.614-8955T>C
|
|
NM_001160277.2:c.669T>C
|
NP_001153749.1:p.His223=
|
|
NR_027689.2:n.626T>C
|
|
|
NR_027690.2:n.758T>C
|
|
|