ENST00000321348.9:c.805G>T
MANE Select
|
ENSP00000319141.4:p.Ala269Ser
|
|
ENST00000321348.8:c.805G>T
|
ENSP00000319141.4:p.Ala269Ser
|
|
ENST00000375252.3:c.*122G>T
|
ENSP00000364401.3:n.*122G>T
|
|
ENST00000409484.5:c.631G>T
|
ENSP00000386739.1:p.Ala211Ser
|
|
NM_001127383.1:c.*122G>T
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NP_001120855.1:n.*122G>T
|
|
NM_001256909.1:c.631G>T
|
NP_001243838.1:p.Ala211Ser
|
|
NM_024843.3:c.805G>T
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NP_079119.3:p.Ala269Ser
|
|
NM_024843.4:c.805G>T
MANE Select
|
NP_079119.3:p.Ala269Ser
|
|
NM_001127383.2:c.*122G>T
|
NP_001120855.1:n.*122G>T
|
|
NM_001256909.2:c.631G>T
|
NP_001243838.1:p.Ala211Ser
|
|