ENST00000684145.1:c.-6G>T
|
ENSP00000508396.1:n.-6G>T
|
|
ENST00000410087.8:c.751G>T
MANE Select
|
ENSP00000386725.3:p.Ala251Ser
|
|
ENST00000339098.9:c.829G>T
|
ENSP00000341159.5:p.Ala277Ser
|
|
ENST00000374967.6:c.687G>T
|
ENSP00000364106.2:n.687G>T
|
|
ENST00000374969.6:c.482-8927G>T
|
ENSP00000364108.2:n.482-8927G>T
|
|
ENST00000374970.6:c.614-8927G>T
|
ENSP00000364109.2:n.614-8927G>T
|
|
ENST00000409440.7:c.697G>T
|
ENSP00000387080.3:p.Ala233Ser
|
|
ENST00000410087.7:c.751G>T
|
ENSP00000386725.3:p.Ala251Ser
|
|
ENST00000421817.5:c.*33G>T
|
ENSP00000411466.1:n.*33G>T
|
|
ENST00000452174.5:c.555G>T
|
ENSP00000409198.1:n.555G>T
|
|
ENST00000479558.5:n.749G>T
|
|
|
ENST00000494398.5:n.751G>T
|
|
|
NM_001030311.2:c.829G>T
|
NP_001025482.1:p.Ala277Ser
|
|
NM_001030312.2:c.482-8927G>T
|
NP_001025483.1:n.482-8927G>T
|
|
NM_001030313.2:c.614-8927G>T
|
NP_001025484.1:n.614-8927G>T
|
|
NM_001160277.1:c.697G>T
|
NP_001153749.1:p.Ala233Ser
|
|
NM_201548.4:c.751G>T
|
NP_963842.1:p.Ala251Ser
|
|
NR_027689.1:n.656G>T
|
|
|
NR_027690.1:n.788G>T
|
|
|
NM_201548.5:c.751G>T
MANE Select
|
NP_963842.1:p.Ala251Ser
|
|
NM_001030311.3:c.829G>T
|
NP_001025482.1:p.Ala277Ser
|
|
NM_001030312.3:c.482-8927G>T
|
NP_001025483.1:n.482-8927G>T
|
|
NM_001030313.3:c.614-8927G>T
|
NP_001025484.1:n.614-8927G>T
|
|
NM_001160277.2:c.697G>T
|
NP_001153749.1:p.Ala233Ser
|
|
NR_027689.2:n.654G>T
|
|
|
NR_027690.2:n.786G>T
|
|
|