ENST00000260950.5:c.526C>G
(MSTN)
MANE Select
|
ENSP00000260950.3:p.Leu176Val
|
|
ENST00000260950.4:c.526C>G
(MSTN)
|
ENSP00000260950.3:p.Leu176Val
|
|
ENST00000478197.1:n.220-18940G>C
(C2orf88)
|
|
|
ENST00000495546.1:n.202-19671G>C
(C2orf88)
|
|
|
NM_005259.2:c.526C>G , LRG_200t1:c.526C>G
(MSTN)
|
NP_005250.1:p.Leu176Val
|
|
XM_005246905.1:c.-359-19671G>C
(C2orf88)
|
XP_005246962.1:n.-359-19671G>C
|
|
XM_011510958.1:c.142C>G
(MSTN)
|
XP_011509260.1:p.Leu48Val
|
|
XM_011511982.1:c.-433-19671G>C
(C2orf88)
|
XP_011510284.1:n.-433-19671G>C
|
|
XM_011511986.1:c.-234-19671G>C
(C2orf88)
|
XP_011510288.1:n.-234-19671G>C
|
|
XM_011511986.2:c.-234-19671G>C
(C2orf88)
|
XP_011510288.1:n.-234-19671G>C
|
|
NM_005259.3:c.526C>G
(MSTN)
MANE Select
|
NP_005250.1:p.Leu176Val
|
|