ENST00000433957.7:c.112G>T
|
ENSP00000411013.3:p.Ala38Ser
|
|
ENST00000644384.2:c.112G>T
MANE Select
|
ENSP00000494414.1:p.Ala38Ser
|
|
ENST00000652415.1:c.112G>T
|
ENSP00000498756.1:p.Ala38Ser
|
|
ENST00000291532.7:c.112G>T
|
ENSP00000291532.3:p.Ala38Ser
|
|
ENST00000398397.3:c.112G>T
|
ENSP00000381434.3:p.Ala38Ser
|
|
ENST00000398405.5:c.106G>T
|
ENSP00000381442.1:p.Ala36Ser
|
|
ENST00000433957.6:c.112G>T
|
ENSP00000411013.2:p.Ala38Ser
|
|
ENST00000482761.1:n.399G>T
|
|
|
NM_001256317.1:c.112G>T
|
NP_001243246.1:p.Ala38Ser
|
|
NM_024022.2:c.112G>T
|
NP_076927.1:p.Ala38Ser
|
|
NM_032405.1:c.112G>T
|
NP_115781.1:p.Ala38Ser
|
|
NR_046020.1:n.1068G>T
|
|
|
NM_001256317.2:c.112G>T
|
NP_001243246.1:p.Ala38Ser
|
|
NM_024022.3:c.112G>T
|
NP_076927.1:p.Ala38Ser
|
|
NM_032405.2:c.112G>T
|
NP_115781.1:p.Ala38Ser
|
|
NM_001256317.3:c.112G>T
MANE Select
|
NP_001243246.1:p.Ala38Ser
|
|
NM_024022.4:c.112G>T
|
NP_076927.1:p.Ala38Ser
|
|