ENST00000684145.1:c.-39G>A
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ENSP00000508396.1:n.-39G>A
|
|
ENST00000410087.8:c.718G>A
MANE Select
|
ENSP00000386725.3:p.Ala240Thr
|
|
ENST00000339098.9:c.796G>A
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ENSP00000341159.5:p.Ala266Thr
|
|
ENST00000374967.6:c.654G>A
|
ENSP00000364106.2:p.Ter218=
|
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ENST00000374969.6:c.482-8960G>A
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ENSP00000364108.2:n.482-8960G>A
|
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ENST00000374970.6:c.614-8960G>A
|
ENSP00000364109.2:n.614-8960G>A
|
|
ENST00000409440.7:c.664G>A
|
ENSP00000387080.3:p.Ala222Thr
|
|
ENST00000410087.7:c.718G>A
|
ENSP00000386725.3:p.Ala240Thr
|
|
ENST00000421817.5:c.522G>A
|
ENSP00000411466.1:p.Ter174=
|
|
ENST00000452174.5:c.522G>A
|
ENSP00000409198.1:p.Ter174=
|
|
ENST00000466715.5:n.534G>A
|
|
|
ENST00000479558.5:n.716G>A
|
|
|
ENST00000494398.5:n.718G>A
|
|
|
NM_001030311.2:c.796G>A
|
NP_001025482.1:p.Ala266Thr
|
|
NM_001030312.2:c.482-8960G>A
|
NP_001025483.1:n.482-8960G>A
|
|
NM_001030313.2:c.614-8960G>A
|
NP_001025484.1:n.614-8960G>A
|
|
NM_001160277.1:c.664G>A
|
NP_001153749.1:p.Ala222Thr
|
|
NM_201548.4:c.718G>A
|
NP_963842.1:p.Ala240Thr
|
|
NR_027689.1:n.623G>A
|
|
|
NR_027690.1:n.755G>A
|
|
|
NM_201548.5:c.718G>A
MANE Select
|
NP_963842.1:p.Ala240Thr
|
|
NM_001030311.3:c.796G>A
|
NP_001025482.1:p.Ala266Thr
|
|
NM_001030312.3:c.482-8960G>A
|
NP_001025483.1:n.482-8960G>A
|
|
NM_001030313.3:c.614-8960G>A
|
NP_001025484.1:n.614-8960G>A
|
|
NM_001160277.2:c.664G>A
|
NP_001153749.1:p.Ala222Thr
|
|
NR_027689.2:n.621G>A
|
|
|
NR_027690.2:n.753G>A
|
|
|