ENST00000265631.10:c.1906C>A
MANE Select
|
ENSP00000265631.6:p.His636Asn
|
|
ENST00000265631.9:c.1906C>A
|
ENSP00000265631.5:p.His636Asn
|
|
ENST00000416240.6:c.1909C>A
|
ENSP00000400101.2:p.His637Asn
|
|
ENST00000494085.1:n.409C>A
|
|
|
NM_001160210.1:c.1909C>A
|
NP_001153682.1:p.His637Asn
|
|
NM_014251.2:c.1906C>A
|
NP_055066.1:p.His636Asn
|
|
NR_027662.1:n.1981C>A
|
|
|
XM_006715831.2:c.1939C>A
|
XP_006715894.1:p.His647Asn
|
|
XM_011515728.1:c.1054C>A
|
XP_011514030.1:p.His352Asn
|
|
XM_006715831.4:c.1939C>A
|
XP_006715894.1:p.His647Asn
|
|
XM_017011663.1:c.1897C>A
|
XP_016867152.1:p.His633Asn
|
|
XM_017011664.2:c.1054C>A
|
XP_016867153.1:p.His352Asn
|
|
XM_017011665.1:c.1054C>A
|
XP_016867154.1:p.His352Asn
|
|
XR_001744525.2:n.2152C>A
|
|
|
XR_002956405.1:n.2710C>A
|
|
|
NM_014251.3:c.1906C>A
MANE Select
|
NP_055066.1:p.His636Asn
|
|
NR_027662.2:n.1932C>A
|
|
|
NM_001160210.2:c.1909C>A
|
NP_001153682.1:p.His637Asn
|
|