ENST00000388913.4:c.856C>T
MANE Select
|
ENSP00000373565.3:p.Pro286Ser
|
|
ENST00000650760.1:c.1459C>T
|
ENSP00000499217.1:p.Pro487Ser
|
|
ENST00000388913.3:c.856C>T
|
ENSP00000373565.3:p.Pro286Ser
|
|
ENST00000395103.2:c.36C>T
|
|
|
NM_198488.3:c.856C>T
|
NP_940890.3:p.Pro286Ser
|
|
XM_005250887.2:c.913C>T
|
XP_005250944.1:p.Pro305Ser
|
|
XM_005250888.2:c.874C>T
|
XP_005250945.1:p.Pro292Ser
|
|
XM_005250889.2:c.856C>T
|
XP_005250946.1:p.Pro286Ser
|
|
XM_011516980.1:c.1177C>T
|
XP_011515282.1:p.Pro393Ser
|
|
XM_011516981.1:c.1024C>T
|
XP_011515283.1:p.Pro342Ser
|
|
XM_005250887.3:c.913C>T
|
XP_005250944.1:p.Pro305Ser
|
|
XM_005250888.3:c.874C>T
|
XP_005250945.1:p.Pro292Ser
|
|
XM_005250889.3:c.856C>T
|
XP_005250946.1:p.Pro286Ser
|
|
XM_011516980.2:c.1459C>T
|
XP_011515282.2:p.Pro487Ser
|
|
XM_011516981.2:c.1024C>T
|
XP_011515283.1:p.Pro342Ser
|
|
XM_024447131.1:c.856C>T
|
XP_024302899.1:p.Pro286Ser
|
|
NM_198488.4:c.856C>T
|
NP_940890.3:p.Pro286Ser
|
|
NM_198488.5:c.856C>T
MANE Select
|
NP_940890.4:p.Pro286Ser
|
|