ENST00000684145.1:c.-46C>T
|
ENSP00000508396.1:n.-46C>T
|
|
ENST00000410087.8:c.711C>T
MANE Select
|
ENSP00000386725.3:p.Ser237=
|
|
ENST00000339098.9:c.789C>T
|
ENSP00000341159.5:p.Ser263=
|
|
ENST00000374967.6:c.647C>T
|
ENSP00000364106.2:p.Ala216Val
|
|
ENST00000374969.6:c.482-8967C>T
|
ENSP00000364108.2:n.482-8967C>T
|
|
ENST00000374970.6:c.614-8967C>T
|
ENSP00000364109.2:n.614-8967C>T
|
|
ENST00000409440.7:c.657C>T
|
ENSP00000387080.3:p.Ser219=
|
|
ENST00000410087.7:c.711C>T
|
ENSP00000386725.3:p.Ser237=
|
|
ENST00000421817.5:c.515C>T
|
ENSP00000411466.1:p.Ala172Val
|
|
ENST00000452174.5:c.515C>T
|
ENSP00000409198.1:p.Ala172Val
|
|
ENST00000466715.5:n.527C>T
|
|
|
ENST00000479558.5:n.709C>T
|
|
|
ENST00000494398.5:n.711C>T
|
|
|
NM_001030311.2:c.789C>T
|
NP_001025482.1:p.Ser263=
|
|
NM_001030312.2:c.482-8967C>T
|
NP_001025483.1:n.482-8967C>T
|
|
NM_001030313.2:c.614-8967C>T
|
NP_001025484.1:n.614-8967C>T
|
|
NM_001160277.1:c.657C>T
|
NP_001153749.1:p.Ser219=
|
|
NM_201548.4:c.711C>T
|
NP_963842.1:p.Ser237=
|
|
NR_027689.1:n.616C>T
|
|
|
NR_027690.1:n.748C>T
|
|
|
NM_201548.5:c.711C>T
MANE Select
|
NP_963842.1:p.Ser237=
|
|
NM_001030311.3:c.789C>T
|
NP_001025482.1:p.Ser263=
|
|
NM_001030312.3:c.482-8967C>T
|
NP_001025483.1:n.482-8967C>T
|
|
NM_001030313.3:c.614-8967C>T
|
NP_001025484.1:n.614-8967C>T
|
|
NM_001160277.2:c.657C>T
|
NP_001153749.1:p.Ser219=
|
|
NR_027689.2:n.614C>T
|
|
|
NR_027690.2:n.746C>T
|
|
|