ENST00000347401.8:c.1604C>A
|
|
|
ENST00000353578.9:c.8341C>A
|
ENSP00000315873.4:p.Pro2781Thr
|
|
ENST00000682957.1:c.1086C>A
|
|
|
ENST00000684508.1:n.1226C>A
|
|
|
ENST00000295550.9:c.8959C>A
MANE Select
|
ENSP00000295550.4:p.Pro2987Thr
|
|
ENST00000295550.8:c.8959C>A
|
ENSP00000295550.4:p.Pro2987Thr
|
|
ENST00000347401.7:c.7135C>A
|
ENSP00000315609.4:p.Pro2379Thr
|
|
ENST00000353578.8:c.8341C>A
|
ENSP00000315873.4:p.Pro2781Thr
|
|
ENST00000409809.5:c.8341C>A
|
ENSP00000386844.1:p.Pro2781Thr
|
|
ENST00000472056.5:c.7138C>A
|
ENSP00000418285.1:p.Pro2380Thr
|
|
ENST00000491769.1:n.5401C>A
|
|
|
NM_004369.3:c.8959C>A , LRG_473t1:c.8959C>A
|
NP_004360.2:p.Pro2987Thr
|
|
NM_057166.4:c.7138C>A
|
NP_476507.3:p.Pro2380Thr
|
|
NM_057167.3:c.8341C>A
|
NP_476508.2:p.Pro2781Thr
|
|
XM_005246065.1:c.8359C>A
|
XP_005246122.1:p.Pro2787Thr
|
|
XM_005246066.1:c.7738C>A
|
XP_005246123.1:p.Pro2580Thr
|
|
XM_006712253.1:c.8458C>A
|
XP_006712316.1:p.Pro2820Thr
|
|
XM_011510574.1:c.8956C>A
|
XP_011508876.1:p.Pro2986Thr
|
|
XM_011510575.1:c.6553C>A
|
XP_011508877.1:p.Pro2185Thr
|
|
XM_017003304.1:c.6553C>A
|
XP_016858793.1:p.Pro2185Thr
|
|
XM_024452684.1:c.7738C>A
|
XP_024308452.1:p.Pro2580Thr
|
|
NM_004369.4:c.8959C>A
MANE Select
|
NP_004360.2:p.Pro2987Thr
|
|
NM_057166.5:c.7138C>A
|
NP_476507.3:p.Pro2380Thr
|
|
NM_057167.4:c.8341C>A
|
NP_476508.2:p.Pro2781Thr
|
|