ENST00000265104.5:c.9802G>T
MANE Select
|
ENSP00000265104.4:p.Ala3268Ser
|
|
ENST00000681290.1:c.9757G>T
|
ENSP00000505288.1:p.Ala3253Ser
|
|
ENST00000265104.4:c.9802G>T
|
ENSP00000265104.4:p.Ala3268Ser
|
|
ENST00000504001.3:n.514G>T
|
|
|
NM_001369.2:c.9802G>T
|
NP_001360.1:p.Ala3268Ser
|
|
XM_005248262.2:c.9757G>T
|
XP_005248319.1:p.Ala3253Ser
|
|
XM_005248262.3:c.9910G>T
|
XP_005248319.2:p.Ala3304Ser
|
|
XM_017009177.1:c.9910G>T
|
XP_016864666.1:p.Ala3304Ser
|
|
XM_017009178.1:c.8815G>T
|
XP_016864667.1:p.Ala2939Ser
|
|
XM_017009179.2:c.8815G>T
|
XP_016864668.1:p.Ala2939Ser
|
|
XM_017009180.1:c.9910G>T
|
XP_016864669.1:p.Ala3304Ser
|
|
XM_017009181.1:c.9910G>T
|
XP_016864670.1:p.Ala3304Ser
|
|
XM_017009182.1:c.9910G>T
|
XP_016864671.1:p.Ala3304Ser
|
|
XM_017009185.1:c.4999G>T
|
XP_016864674.1:p.Ala1667Ser
|
|
XM_017009186.1:c.4552G>T
|
XP_016864675.1:p.Ala1518Ser
|
|
XM_017009188.1:c.3889G>T
|
XP_016864677.1:p.Ala1297Ser
|
|
XM_024454388.1:c.8815G>T
|
XP_024310156.1:p.Ala2939Ser
|
|
XM_024454389.1:c.8404G>T
|
XP_024310157.1:p.Ala2802Ser
|
|
NM_001369.3:c.9802G>T
MANE Select
|
NP_001360.1:p.Ala3268Ser
|
|