ENST00000494137.2:c.661G>T
|
ENSP00000510626.1:p.Ala221Ser
|
|
ENST00000498257.6:c.661G>T
|
ENSP00000510533.1:p.Ala221Ser
|
|
ENST00000617695.5:c.8584G>T
|
ENSP00000481744.2:p.Ala2862Ser
|
|
ENST00000618192.5:c.8860G>T
|
ENSP00000480802.2:p.Ala2954Ser
|
|
ENST00000688198.1:n.1574G>T
|
|
|
ENST00000688799.1:c.661G>T
|
ENSP00000508458.1:p.Ala221Ser
|
|
ENST00000690858.1:n.1590G>T
|
|
|
ENST00000693461.1:n.933G>T
|
|
|
ENST00000421865.3:c.8596G>T
MANE Select
|
ENSP00000400365.2:p.Ala2866Ser
|
|
ENST00000421865.2:c.8596G>T
|
ENSP00000400365.2:p.Ala2866Ser
|
|
ENST00000617695.4:c.8584G>T
|
ENSP00000481744.1:p.Ala2862Ser
|
|
ENST00000618192.4:c.8593G>T
|
ENSP00000480802.1:p.Ala2865Ser
|
|
NM_000426.3:c.8596G>T , LRG_409t1:c.8596G>T
|
NP_000417.2:p.Ala2866Ser
|
|
NM_001079823.1:c.8584G>T
|
NP_001073291.1:p.Ala2862Ser
|
|
XM_005266981.2:c.8860G>T
|
XP_005267038.1:p.Ala2954Ser
|
|
XM_005266982.2:c.8848G>T
|
XP_005267039.1:p.Ala2950Ser
|
|
XM_011535820.1:c.8854G>T
|
XP_011534122.1:p.Ala2952Ser
|
|
XR_942984.1:n.1461-2457C>A
|
|
|
XR_942985.1:n.1325-2457C>A
|
|
|
XM_005266981.3:c.8860G>T
|
XP_005267038.1:p.Ala2954Ser
|
|
XM_005266982.3:c.8848G>T
|
XP_005267039.1:p.Ala2950Ser
|
|
XM_011535820.2:c.8854G>T
|
XP_011534122.1:p.Ala2952Ser
|
|
XM_017010851.2:c.8866G>T
|
XP_016866340.1:p.Ala2956Ser
|
|
XM_017010852.1:c.6991G>T
|
XP_016866341.1:p.Ala2331Ser
|
|
XR_001743859.1:n.3901-2457C>A
|
|
|
XR_001743860.1:n.1180-2457C>A
|
|
|
XR_001743861.1:n.1347-2457C>A
|
|
|
XR_001743863.1:n.883-2457C>A
|
|
|
XR_002956395.1:n.9132-2457C>A
|
|
|
XR_002956396.1:n.3127-2457C>A
|
|
|
NM_000426.4:c.8596G>T
MANE Select
|
NP_000417.3:p.Ala2866Ser
|
|
NM_001079823.2:c.8584G>T
|
NP_001073291.2:p.Ala2862Ser
|
|