ENST00000347401.8:c.1475C>T
|
|
|
ENST00000353578.9:c.8212C>T
|
ENSP00000315873.4:p.Pro2738Ser
|
|
ENST00000682957.1:c.957C>T
|
|
|
ENST00000684508.1:n.1097C>T
|
|
|
ENST00000295550.9:c.8830C>T
MANE Select
|
ENSP00000295550.4:p.Pro2944Ser
|
|
ENST00000295550.8:c.8830C>T
|
ENSP00000295550.4:p.Pro2944Ser
|
|
ENST00000347401.7:c.7006C>T
|
ENSP00000315609.4:p.Pro2336Ser
|
|
ENST00000353578.8:c.8212C>T
|
ENSP00000315873.4:p.Pro2738Ser
|
|
ENST00000409809.5:c.8212C>T
|
ENSP00000386844.1:p.Pro2738Ser
|
|
ENST00000472056.5:c.7009C>T
|
ENSP00000418285.1:p.Pro2337Ser
|
|
ENST00000491769.1:n.5272C>T
|
|
|
NM_004369.3:c.8830C>T , LRG_473t1:c.8830C>T
|
NP_004360.2:p.Pro2944Ser
|
|
NM_057166.4:c.7009C>T
|
NP_476507.3:p.Pro2337Ser
|
|
NM_057167.3:c.8212C>T
|
NP_476508.2:p.Pro2738Ser
|
|
XM_005246065.1:c.8230C>T
|
XP_005246122.1:p.Pro2744Ser
|
|
XM_005246066.1:c.7609C>T
|
XP_005246123.1:p.Pro2537Ser
|
|
XM_006712253.1:c.8329C>T
|
XP_006712316.1:p.Pro2777Ser
|
|
XM_011510574.1:c.8827C>T
|
XP_011508876.1:p.Pro2943Ser
|
|
XM_011510575.1:c.6424C>T
|
XP_011508877.1:p.Pro2142Ser
|
|
XM_017003304.1:c.6424C>T
|
XP_016858793.1:p.Pro2142Ser
|
|
XM_024452684.1:c.7609C>T
|
XP_024308452.1:p.Pro2537Ser
|
|
NM_004369.4:c.8830C>T
MANE Select
|
NP_004360.2:p.Pro2944Ser
|
|
NM_057166.5:c.7009C>T
|
NP_476507.3:p.Pro2337Ser
|
|
NM_057167.4:c.8212C>T
|
NP_476508.2:p.Pro2738Ser
|
|