ENST00000225964.10:c.3175C>T
MANE Select
|
ENSP00000225964.6:p.Pro1059Ser
|
|
ENST00000225964.9:c.3175C>T
|
ENSP00000225964.5:p.Pro1059Ser
|
|
ENST00000511732.1:n.119C>T
|
|
|
NM_000088.3:c.3175C>T , LRG_1t1:c.3175C>T
|
NP_000079.2:p.Pro1059Ser
|
|
XM_005257058.3:c.2905C>T
|
XP_005257115.2:p.Pro969Ser
|
|
XM_005257059.3:c.2257C>T
|
XP_005257116.2:p.Pro753Ser
|
|
XM_011524341.1:c.2977C>T
|
XP_011522643.1:p.Pro993Ser
|
|
XM_005257058.4:c.2905C>T
|
XP_005257115.2:p.Pro969Ser
|
|
XM_005257059.4:c.2257C>T
|
XP_005257116.2:p.Pro753Ser
|
|
NM_000088.4:c.3175C>T
MANE Select
|
NP_000079.2:p.Pro1059Ser
|
|