ENST00000643759.2:c.7021G>T
MANE Select
|
ENSP00000495214.1:p.Ala2341Ser
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|
ENST00000368147.8:c.7021G>T
|
ENSP00000357129.4:p.Ala2341Ser
|
|
ENST00000481212.5:n.462G>T
|
|
|
ENST00000498708.1:n.453G>T
|
|
|
ENST00000614909.4:c.7021G>T
|
ENSP00000482595.1:p.Ala2341Ser
|
|
NM_003126.2:c.7021G>T
|
NP_003117.2:p.Ala2341Ser
|
|
XM_011509916.1:c.7021G>T
|
XP_011508218.1:p.Ala2341Ser
|
|
XM_011509917.1:c.7003G>T
|
XP_011508219.1:p.Ala2335Ser
|
|
NM_003126.3:c.7021G>T
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NP_003117.2:p.Ala2341Ser
|
|
XM_011509916.2:c.7021G>T
|
XP_011508218.1:p.Ala2341Ser
|
|
XM_011509917.3:c.7003G>T
|
XP_011508219.1:p.Ala2335Ser
|
|
NM_003126.4:c.7021G>T
MANE Select
|
NP_003117.2:p.Ala2341Ser
|
|