ENST00000347401.8:c.1278C>G
|
|
|
ENST00000353578.9:c.8015C>G
|
ENSP00000315873.4:p.Thr2672Ser
|
|
ENST00000682957.1:c.760C>G
|
|
|
ENST00000684508.1:n.900C>G
|
|
|
ENST00000295550.9:c.8633C>G
MANE Select
|
ENSP00000295550.4:p.Thr2878Ser
|
|
ENST00000295550.8:c.8633C>G
|
ENSP00000295550.4:p.Thr2878Ser
|
|
ENST00000347401.7:c.6809C>G
|
ENSP00000315609.4:p.Thr2270Ser
|
|
ENST00000353578.8:c.8015C>G
|
ENSP00000315873.4:p.Thr2672Ser
|
|
ENST00000409809.5:c.8015C>G
|
ENSP00000386844.1:p.Thr2672Ser
|
|
ENST00000472056.5:c.6812C>G
|
ENSP00000418285.1:p.Thr2271Ser
|
|
ENST00000491769.1:n.5075C>G
|
|
|
NM_004369.3:c.8633C>G , LRG_473t1:c.8633C>G
|
NP_004360.2:p.Thr2878Ser
|
|
NM_057166.4:c.6812C>G
|
NP_476507.3:p.Thr2271Ser
|
|
NM_057167.3:c.8015C>G
|
NP_476508.2:p.Thr2672Ser
|
|
XM_005246065.1:c.8033C>G
|
XP_005246122.1:p.Thr2678Ser
|
|
XM_005246066.1:c.7412C>G
|
XP_005246123.1:p.Thr2471Ser
|
|
XM_006712253.1:c.8132C>G
|
XP_006712316.1:p.Thr2711Ser
|
|
XM_011510574.1:c.8630C>G
|
XP_011508876.1:p.Thr2877Ser
|
|
XM_011510575.1:c.6227C>G
|
XP_011508877.1:p.Thr2076Ser
|
|
XM_017003304.1:c.6227C>G
|
XP_016858793.1:p.Thr2076Ser
|
|
XM_024452684.1:c.7412C>G
|
XP_024308452.1:p.Thr2471Ser
|
|
NM_004369.4:c.8633C>G
MANE Select
|
NP_004360.2:p.Thr2878Ser
|
|
NM_057166.5:c.6812C>G
|
NP_476507.3:p.Thr2271Ser
|
|
NM_057167.4:c.8015C>G
|
NP_476508.2:p.Thr2672Ser
|
|