ENST00000370096.9:c.2636G>A
MANE Select
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ENSP00000359114.3:p.Arg879Gln
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|
ENST00000353414.8:c.2519G>A
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ENSP00000302551.6:p.Arg840Gln
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|
ENST00000358392.6:c.2672G>A
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ENSP00000351163.2:p.Arg891Gln
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|
ENST00000370096.7:c.2636G>A
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ENSP00000359114.3:p.Arg879Gln
|
|
ENST00000512756.5:c.2288G>A
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ENSP00000426533.1:p.Arg763Gln
|
|
ENST00000635193.1:c.1970G>A
|
|
|
NM_001190709.1:c.2519G>A
|
NP_001177638.1:p.Arg840Gln
|
|
NM_001854.3:c.2636G>A
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NP_001845.3:p.Arg879Gln
|
|
NM_080629.2:c.2672G>A
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NP_542196.2:p.Arg891Gln
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|
NM_080630.3:c.2288G>A
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NP_542197.3:p.Arg763Gln
|
|
XM_011540719.1:c.2636G>A
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XP_011539021.1:p.Arg879Gln
|
|
XM_011540720.1:c.869G>A
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XP_011539022.1:p.Arg290Gln
|
|
XM_011540721.1:c.224G>A
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XP_011539023.1:p.Arg75Gln
|
|
XR_946545.1:n.3050G>A
|
|
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NR_134980.1:n.2970G>A
|
|
|
XM_017000334.1:c.2789G>A
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XP_016855823.1:p.Arg930Gln
|
|
XM_017000335.1:c.2783G>A
|
XP_016855824.1:p.Arg928Gln
|
|
XM_017000336.1:c.2789G>A
|
XP_016855825.1:p.Arg930Gln
|
|
XM_017000337.1:c.1187G>A
|
XP_016855826.1:p.Arg396Gln
|
|
NM_001854.4:c.2636G>A
MANE Select
|
NP_001845.3:p.Arg879Gln
|
|
NM_080630.4:c.2288G>A
|
NP_542197.3:p.Arg763Gln
|
|
NR_134980.2:n.2996G>A
|
|
|
NM_001190709.2:c.2519G>A
|
NP_001177638.1:p.Arg840Gln
|
|
NM_080629.3:c.2672G>A
|
NP_542196.2:p.Arg891Gln
|
|