ENST00000696142.1:c.*746G>T
|
ENSP00000512434.1:n.*746G>T
|
|
ENST00000696143.1:c.1205G>T
|
ENSP00000512435.1:n.1205G>T
|
|
ENST00000696153.1:c.*427G>T
|
ENSP00000512444.1:n.*427G>T
|
|
ENST00000256474.3:c.*427G>T
MANE Select
|
ENSP00000256474.3:n.*427G>T
|
|
ENST00000256474.2:c.*427G>T
|
ENSP00000256474.2:n.*427G>T
|
|
ENST00000345392.2:c.*427G>T
|
ENSP00000344757.2:n.*427G>T
|
|
NM_000551.3:c.*427G>T , LRG_322t1:c.*427G>T
|
NP_000542.1:n.*427G>T
|
|
NM_198156.2:c.*427G>T
|
NP_937799.1:n.*427G>T
|
|
NM_001354723.1:c.*623G>T
|
NP_001341652.1:n.*623G>T
|
|
NM_000551.4:c.*427G>T
MANE Select
|
NP_000542.1:n.*427G>T
|
|
NM_001354723.2:c.*623G>T
|
NP_001341652.1:n.*623G>T
|
|
NM_198156.3:c.*427G>T
|
NP_937799.1:n.*427G>T
|
|